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LipoLume (10mL × 5 Vials)
7900
$79.00
Unit price perLipoLume (10mL × 5 Vials)
7900
$79.00
Unit price per
Product Identification
LipoLume
Advanced Lipolytic Solution
Phace Global Co., Ltd. Sterile Liquid Solution
Total Volume/Content
50mL per box (10mL × 5 Vials)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
- Lecithin: Natural emulsifier that disrupts fat cell membranes.
- Riboflavin (Vitamin B2): Activates fat metabolism (turns fat into energy) and provides anti-inflammatory benefits.
- Bromelain: Pineapple-derived enzyme for protein breakdown, reducing swelling and inflammation.
Supportive Complex
- Peptides: Acetyl Hexapeptide-8, Palmitoyl Pentapeptide-4, Palmitoyl Tetrapeptide-7 (Skin firming).
- Antioxidants: Glutathione, Ascorbic Acid, Carnitine, Adenosine.
- Natural Extracts: Centella Asiatica, Chamomilla, Salvia, Scutellaria.
Mechanism of Action
Step 1: Lecithin disrupts fat cells. Step 2: Riboflavin boosts metabolism of released fat. Step 3: Bromelain supports drainage and reduces swelling.
Lecithin Riboflavin (B2) Bromelain Painless Formula
Efficacy & Benefits
Main Effects
- Dual Action: Fat reduction combined with skin firming to prevent sagging.
- Contouring: Defines facial and body lines by removing stubborn fat.
- Reduced Downtime: Formulated to cause minimal pain and swelling compared to traditional PPC.
- Brightening: Improves skin tone via Riboflavin.
Targeted Areas
Double Chin Jawline Abdomen Love Handles Arms Thighs
Usage Protocol
Method
Subcutaneous Injection
| Area | Injection Depth | Volume per Area | Point Volume / Interval |
|---|---|---|---|
|
Face (Chin, Jawline) |
2–4 mm | 4–10 cc | 0.2–0.3 cc / 0.5–1 cm |
|
Body (Abdomen, Arms) |
6–12 mm | 10–50 cc | 1.0–2.0 cc / 1.5–2.0 cm |
Treatment Cycle
3–5 sessions spaced 7–10 days apart.
Preparation
Ready-to-use solution. Can be mixed with small amounts of Lidocaine if needed for comfort.
Product Strategy
Premium Natural Enzyme
LipoLume is positioned as a painless, no-swelling alternative to traditional PPC lipolytics. It is ideal for patients who require effective fat reduction but are concerned about downtime or inflammation.
Storage & Handling
Light Sensitive Riboflavin is light-sensitive. Keep vials in the box and away from direct light.
Frequently Asked Questions
What is LipoLume used for?
LipoLume is an advanced lipolytic solution for fat reduction and facial and body contouring, targeting areas such as the double chin, jawline, abdomen, love handles, arms, and thighs.
What are the primary active ingredients?
The primary active ingredients are Lecithin (which disrupts fat cell membranes), Riboflavin / Vitamin B2 (which activates fat metabolism), and Bromelain (a pineapple-derived enzyme that reduces swelling and inflammation).
How many sessions are recommended and how is it administered?
LipoLume is administered by subcutaneous injection, with a treatment cycle of 3–5 sessions spaced 7–10 days apart. It is a ready-to-use solution that can be mixed with small amounts of Lidocaine if needed for comfort.
Who manufactures LipoLume?
LipoLume is manufactured by Phace Global Co., Ltd.
LIPORASE Inj (1.0mL × 10 Vials)
3750
$37.50
Unit price perLIPORASE Inj (1.0mL × 10 Vials)
3750
$37.50
Unit price per
HYALURONIDASE INJECTION
LIPORASE inj
10 Vials per Box
Professional Hyaluronidase for Filler Correction & Lipolysis Enhancement
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧩 Product Overview
Advanced Corrective Enzyme Solution
LIPORASE inj is a specialized depolymerizing enzyme formulation containing 1,500 IU of Hyaluronidase per vial. This professional-grade solution effectively dissolves hyaluronic acid dermal fillers while enhancing the efficacy of fat-dissolving treatments. Each lyophilized powder vial ensures optimal stability and precision in corrective aesthetic procedures.
Active Enzyme
1,500
IU
Hyaluronidase (EP) per vial
Formulation
Lyophilized
Powder
Package Size
10
Vials
Complete treatment box
Storage
Below 25°C
Room Temp
Immediate Results Within 24-48 Hours
📋 Detailed Specifications
| Specification Category | Details/Values | Additional Information |
|---|---|---|
| Active Ingredient | Hyaluronidase (EP) 1500 IU | Depolymerizing enzyme |
| Stabilizing Agent | Lactose Hydrate 13.3 mg | Per vial formulation |
| Dissolution Capacity | 3cc HA Filler | Per vial with 3cc saline |
| Effect Timeline | Immediate to 24-48 hours | Complete dissolution period |
| Administration Route | Subcutaneous/Dermal Injection | Professional application required |
| Reconstitution | Sterile Saline Solution | 3-5cc depending on application |
🧬 Ingredients & Composition
Hyaluronidase (EP)A specialized depolymerizing enzyme that specifically targets and breaks down the molecular bonds of hyaluronic acid. This enzyme reduces the viscosity and volume of HA fillers, allowing the body to naturally metabolize and absorb the broken-down components while leaving natural HA intact.Lactose HydrateA pharmaceutical-grade stabilizing agent that maintains the integrity and stability of the lyophilized enzyme powder, ensuring consistent potency and effectiveness throughout the product's shelf life.Lyophilized FormulationAdvanced freeze-drying technology preserves the enzyme's biological activity while providing extended stability and precise dosing control for professional applications.
Active
Hyaluronidase (EP)
1,500 IU
Primary depolymerizing enzyme that specifically targets hyaluronic acid molecular bonds. This highly purified enzyme maintains selective activity against synthetic HA fillers while preserving the body's natural hyaluronic acid, ensuring targeted correction without systemic effects.
Stabilizer
Lactose Hydrate
13.3 mg
Pharmaceutical-grade excipient that maintains enzyme stability in lyophilized form and facilitates smooth reconstitution with saline solution, ensuring consistent enzyme activity and optimal therapeutic outcomes.
💡 Clinical Benefits & Applications
Filler Correction Applications
Effectively reverses poorly placed, overfilled, or unevenly distributed HA dermal fillers. Resolves nodular formations and granulomas caused by filler complications. Essential for emergency treatment of vascular occlusion cases.
Immediate Dissolution Selective Action Emergency Use
Lipolysis Enhancement
Synergistically enhances fat-dissolving injection effectiveness by improving tissue diffusion and penetration. Aids in cellulite reduction and improves overall treatment outcomes when combined with lipolytic agents.
- Enhanced diffusion of fat-dissolving agents throughout target tissue
- Improved treatment efficacy for stubborn adipose deposits
- Reduction in fibrous cellulite through tissue matrix modification
- Accelerated treatment response and visible results
Professional Versatility
Dual-purpose formulation suitable for both corrective aesthetic procedures and enhancement of body contouring treatments. Compatible with various injection techniques and treatment protocols.
🧪 Usage Protocols & Application Guide
1
Preparation & Assessment
Assess the target area and determine the appropriate application protocol. For filler dissolution, evaluate the volume and depth of HA filler. For lipolysis enhancement, prepare the treatment cocktail and determine injection sites.
2
Reconstitution Process
Reconstitute the lyophilized powder with sterile saline: 3cc saline for filler dissolution or 5cc saline for fat-dissolving synergy. Ensure complete dissolution before application.
3
Injection Technique
Administer via subcutaneous or superficial dermal injection using appropriate needle gauge. For filler correction, inject directly into the filler deposit. For lipolysis, distribute evenly throughout the treatment area.
4
Post-Treatment Monitoring
Monitor patient response and effects. Initial results appear immediately with full effects visible within 24-48 hours. Schedule follow-up assessment and additional treatment if required.
📊 Specific Application Protocols
| Application Type | Reconstitution Ratio | Target Area | Expected Outcome |
|---|---|---|---|
| Filler Dissolution | 1 vial + 3cc saline | HA filler deposits | Dissolves ~3cc HA filler |
| Lipolysis Enhancement | 1 vial + 5cc saline | Adipose tissue | Enhanced fat dissolution |
| Emergency Correction | 1 vial + 3cc saline | Vascular occlusion area | Immediate filler breakdown |
| Cellulite Treatment | 1 vial + 5cc saline | Fibrous cellulite areas | Improved skin texture |
Important Safety Information
Professional use only. This product requires proper medical training and sterile injection techniques for safe and effective application.
- Contraindicated in patients with known hyaluronidase allergy
- Do not use on infected areas or near recent botulinum toxin injection sites
- Store in sealed container at room temperature below 25°C, away from direct sunlight
- Use the reconstituted solution immediately; storing reconstituted product is not recommended
- Perform patch test before full treatment to assess allergic reactions
- Avoid strenuous exercise, sun exposure, and alcohol for 24-48 hours post-treatment
🎯 Target Applications & Recommendations
| Target Application | Symptoms/Situation | Usage Classification | Clinical Reason |
|---|---|---|---|
| Corrective Use | Overfilling, unevenness, incorrect HA filler placement | Filler Dissolution | Hyaluronidase specifically breaks down hyaluronic acid bonds |
| Supportive Use | Enhancing lipolysis procedures, reducing fibrous cellulite | Fat-Dissolving Synergy | Facilitates dispersion and efficacy of fat-dissolving agents |
| Emergency Use | Vascular occlusion from filler injection | Immediate Intervention | Rapid dissolution to restore vascular flow |
Which Application is Right for You?
Based on your specific clinical needs and treatment goals, LIPORASE inj offers versatile solutions for both corrective and enhancement procedures. Choose the appropriate protocol focusing on your main concerns such as filler correction, body contouring enhancement, or emergency intervention.
🔹 Comprehensive Product Details
Professional Filler Dissolution ProtocolFor correcting unsatisfactory HA filler results: Reconstitute 1 vial with 3cc saline to create a solution capable of dissolving approximately 3cc of HA filler. Effects begin almost immediately with complete dissolution within 24-48 hours.Lipolysis Enhancement ProtocolFor improving fat-dissolving treatments: Mix 1 vial with 5cc saline and combine with fat-dissolving cocktail to enhance spread and efficacy throughout target adipose tissue, resulting in improved treatment outcomes.Emergency Intervention ProtocolFor vascular occlusion cases: Immediate injection around affected area using standard dissolution protocol to rapidly break down filler material and restore proper blood circulation.Treatment Depth GuidelinesInjection depth should target the superficial dermal or subcutaneous layer depending on the original filler placement or treatment objective. Precise technique ensures optimal results and patient safety.
📦 Storage & Handling Requirements
Storage Temperature
Below 25°C
Room Temp
Hermetic container, away from direct sunlight
After Reconstitution
Immediate
Use
Use immediately; storing reconstituted product is not recommended
Original Package
Stable
Long-term
Lyophilized powder form
Patch Test
Required
Pre-treatment
Allergy assessment recommended
👨⚕️ Professional Guidelines
Pre-Treatment Assessment
Comprehensive evaluation of treatment area, patient medical history, and previous filler applications. Document filler type, volume, and injection sites for optimal treatment planning.
- Verify type and volume of existing HA fillers
- Assess patient's allergy history and previous reactions
- Evaluate treatment area for signs of infection or inflammation
- Plan injection strategy based on filler depth and distribution
Treatment Execution
Professional injection techniques ensuring patient safety and optimal therapeutic outcomes. Proper sterile technique and precise dosing are essential for successful results.
- Use sterile injection technique with appropriate needle gauge
- Monitor patient response during and immediately after injection
- Document treatment parameters and patient response
- Provide clear post-treatment care instructions
Post-Treatment Monitoring
Systematic follow-up to ensure treatment effectiveness and patient satisfaction. Assessment of results and planning for additional treatments if necessary.
- Evaluate treatment response at 24-48 hour follow-up
- Document photographic evidence of treatment outcomes
- Assess need for additional treatment sessions
- Monitor for any adverse reactions or complications
✅ Quality Assurance & Manufacturing
Manufacturer
Daehan New Pharm
Certified
Testing Standard
European Pharmacopoeia
EP Grade
Purity Level
Pharmaceutical
Grade
Product Status
Genuine
Authentic
📄 Technical Summary
1,500 IU Hyaluronidase Per Vial
Complete Package Contents10 vials of lyophilized Hyaluronidase powder (1,500 IU each), sterile packaging, and comprehensive professional usage guidelines for optimal treatment outcomes.Reconstitution RequirementsSterile saline solution required for reconstitution. Volume depends on intended use: 3cc for filler dissolution, 5cc for lipolysis enhancement protocols.Professional ConsultationProfessional medical consultation and proper injection training are essential for safe and effective use. Not suitable for home use or non-professional application.Compatibility InformationCompatible with most fat-dissolving solutions and can be combined with lidocaine to minimize injection discomfort. Do not use near recent botulinum toxin injection sites.
❓ Frequently Asked Questions
Keywords: Hyaluronidase, Dermal Filler Dissolver, Filler Correction, HA Filler Reversal, Fat-Dissolving Synergy, Cellulite Reduction, Vascular Occlusion, Corrective Enzyme, Lipolysis Enhancer, Daehan New Pharm, Genuine, Professional Use, Emergency Intervention, Aesthetic Medicine
Lipotocin Inj (12mL x 10 Amps)
5200
$52.00
Unit price perLipotocin Inj (12mL x 10 Amps)
5200
$52.00
Unit price per
Product Identification
Lipotocin Inj.
High Dose Cinderella Injection
South Korean Manufacturer IV Injection Ampoule
Total Volume/Content
120mL per box (12mL × 10 Ampoules)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
Thioctic Acid (Alpha-Lipoic Acid) 300mg
Mechanism of Action
Thioctic Acid acts as an antioxidant master, regenerating Vitamin C, E, and Glutathione while scavenging free radicals. It also increases mitochondrial energy expenditure to aid in lipolysis (fat breakdown) and prevents protein glycation to reduce tissue aging.
Thioctic Acid 300mg High Dose Metabolic Activation Anti-Glycation
Efficacy & Benefits
Main Effects
- Intensive Anti-Aging: Powerful antioxidant protection against cellular damage.
- Skin Brightening: Reduces dullness and improves skin texture ("Baby Face Injection").
- Body Slimming: Boosts metabolism to aid in weight loss and reduce edema.
- Fatigue Recovery: Improves energy levels and exhaustion.
- Diabetic Neuropathy Relief: Relieves sensory abnormalities.
Targeted Use
Systemic IV Drip Skin Tone Improvement Metabolic Boost
Usage Protocol
Dilution Required Do not inject undiluted directly ("IV Push") as it causes vascular pain and potential shock.
Application Method
Intravenous Drip (IV Infusion)
Dilution Protocol
Mix 1 ampoule (12mL) with 100mL – 250mL of Normal Saline.
Infusion Speed
Administer slowly over at least 15–30 minutes.
Treatment Cycle
1–2 times per week; standard course of 10 sessions.
Product Comparison
| Product Version | Thioctic Acid Content | Primary Strategy |
|---|---|---|
| Lipotocin (High Dose) | 300mg / 12mL | Intensive Slimming & Metabolic Boost |
| Standard Cindella (Low Dose) | 25mg / 5mL | Cocktail Maintenance (Mixed with Vit C/Glutathione) |
Storage & Handling
Required Storage Temperature
Room temperature (1°C – 30°C)
Light Sensitivity
Strictly Protect from Light. Keep ampoules in the original box until use.
Shelf Life
24–36 months from manufacture date
Precautions & Safety
Contraindications Do not use in children/adolescents or patients with hypersensitivity to Thioctic Acid.
Safety Warnings Rapid infusion can cause headache, nausea, and respiratory distress. Diabetics should monitor glucose levels as Thioctic acid may cause hypoglycemia.
Common Temporary Side Effects
- Nausea, vomiting, or gastrointestinal discomfort (rare with slow drip).
- Skin rash or itching at the injection site.
Post-Treatment Care
Avoid heavy alcohol consumption as it interferes with metabolic effects.
Frequently Asked Questions
What is Lipotocin Inj. used for?
Lipotocin Inj. is a high-dose Thioctic Acid (Cinderella) injection used for intensive anti-aging antioxidant protection, skin brightening, body slimming through metabolic boost and edema reduction, fatigue recovery, and relief of diabetic neuropathy (sensory abnormalities).
What is Lipotocin's active ingredient?
The primary active ingredient is Thioctic Acid (Alpha-Lipoic Acid) at 300mg per 12mL ampoule. It acts as an antioxidant master, regenerating Vitamins C and E and Glutathione, increasing mitochondrial energy expenditure to aid lipolysis, and preventing protein glycation.
How is Lipotocin administered?
Lipotocin is administered as an intravenous drip (IV infusion). One ampoule (12mL) is diluted with 100mL–250mL of normal saline and infused slowly over at least 15–30 minutes. It must not be injected undiluted as an IV push, which can cause vascular pain and potential shock. The standard cycle is 1–2 times per week for a course of 10 sessions.
Who should not use Lipotocin and what are the precautions?
Lipotocin is contraindicated in children and adolescents and in patients with hypersensitivity to Thioctic Acid. Rapid infusion can cause headache, nausea, and respiratory distress, and diabetics should monitor glucose levels as Thioctic Acid may cause hypoglycemia. Heavy alcohol consumption should be avoided as it interferes with the metabolic effects.
Keywords
Lipotocin Thioctic Acid 300mg Alpha Lipoic Acid High Dose Cindella Cinderella Injection Fat Burn Injection Antioxidant IV Metabolism Booster
LIPOVELA PPC Solution (10mL × 10 Vials)
5700
$57.00
Unit price perLIPOVELA PPC Solution (10mL × 10 Vials)
5700
$57.00
Unit price perFat Dissolving Solution
LIPOVELA PPC Solution
10ml × 10 Vials per Box
Advanced Fat Dissolving Injectable for Body & Facial Contouring
LIPOVELA Product Package Visual
LIPOVELA PPC Solution is a professional-grade fat dissolving injectable designed for targeted reduction of localized fat deposits. Featuring a powerful combination of Phosphatidylcholine, Sodium Deoxycholate, and metabolism-enhancing compounds, this solution provides effective body and facial contouring with enhanced skin elasticity and improved lymphatic circulation. Available in two specialized formulations for optimal results in different treatment areas.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
01
Active Ingredients & Composition
-
Phosphatidylcholine (PPC)Essential phospholipid that penetrates and dissolves fat cell membranes, facilitating the breakdown of adipose tissue for natural elimination through the lymphatic system.Active
-
Sodium DeoxycholateBile acid derivative that acts as a detergent to destroy fat cell membranes, enabling the breakdown and metabolism of localized fat deposits.Active
-
L-CarnitineAmino acid derivative that accelerates fat metabolism by promoting the transport of fatty acids into mitochondria for energy conversion.Enhancer
-
Riboflavin (Vitamin B2)Essential vitamin that supports energy metabolism and cellular regeneration processes, enhancing the overall effectiveness of fat breakdown.Support
-
Cyanocobalamin (Vitamin B12)Crucial vitamin for metabolic processes and cellular energy production, supporting the body's natural fat elimination mechanisms.Support
Ingredient Mechanism of Action Diagram
Advanced Formulation Technology
The synergistic combination of membrane-disrupting agents and metabolism enhancers creates a comprehensive fat dissolution system. Sodium deoxycholate breaks down fat cell walls, while PPC facilitates membrane penetration. L-Carnitine and B vitamins accelerate the metabolic processing of released fatty acids, ensuring efficient elimination and enhanced treatment outcomes.
02
Treatment Benefits & Expected Effects
Localized Fat Reduction
Targeted breakdown and elimination of stubborn fat deposits in problem areas resistant to diet and exercise, resulting in improved body contours and reduced volume.
Visible Progressive
Enhanced Body & Facial Contouring
Improvement in overall silhouette definition and facial profile refinement, creating more sculpted and aesthetically pleasing contours in treated areas.
Sculpting Defining
Skin Elasticity Enhancement
Stimulation of collagen production and tissue regeneration leading to improved skin firmness, texture, and elasticity in treated areas.
Firming Tightening
Lymphatic Circulation Support
Enhancement of lymphatic drainage and circulation, promoting efficient elimination of metabolized fat and reducing water retention.
Detoxifying Draining
-
✓Non-surgical alternative to liposuction with minimal downtime and recovery
-
✓Dual-action formula combining fat dissolution with skin enhancement benefits
-
✓Pre-mixed solution for simplified preparation and consistent treatment delivery
-
✓Specialized formulations optimized for different treatment areas and patient needs
Before and After Treatment Results
03
Application Protocol & Usage Guidelines
1
Patient Assessment & Area Preparation
Conduct thorough evaluation of treatment areas, mark injection sites, and prepare skin with appropriate antiseptic protocols. Ensure patient suitability and discuss expected outcomes.
2
Solution Preparation & Equipment Setup
Prepare LIPOVELA solution at room temperature, select appropriate needle gauge, and ensure all injection equipment is sterile and ready for application.
3
Subcutaneous Injection Application
Inject 0.05-0.2cc per point into subcutaneous fat layer with injection points spaced approximately 1cm apart. Use appropriate volume per treatment area as specified in protocol guidelines.
4
Post-Treatment Assessment
Monitor immediate treatment response, provide post-care instructions, and schedule appropriate follow-up appointments based on individual response and treatment protocol.
5
Follow-up Care & Monitoring
Provide comprehensive aftercare guidance including hydration recommendations, activity restrictions, and monitoring instructions for optimal treatment outcomes and patient safety.
Injection Technique and Treatment Area Guide
LIPOVELA Body Treatment Protocol
Standard Method
Treatment Areas: Abdomen, thighs, arms, waist. Recommended Sessions: 2-3 treatments with 15-day intervals. Dosage: Up to 10ml per treatment site per session. Target Areas: Broad area localized fat deposits resistant to conventional methods.
LIPOVELA-V Facial Contouring Protocol
Specialized Method
Treatment Areas: Double chin, jawline, jowls. Recommended Sessions: 2-4 treatments with 4-6 week intervals. Dosage: 2-4ml per facial area per session. Enhanced Formula: Contains growth factors (EGF, FGF, IGF) for additional skin lifting and anti-aging benefits.
04
Product Specifications & Variants
| Product Version | Target Area | Key Focus | Dosage Range | Notable Features |
|---|---|---|---|---|
| LIPOVELA (Body) | Abdomen, Thighs, Arms, Waist | PPC, Deoxycholate, L-Carnitine, B-Vitamins | Up to 10ml per site | Concentrated formula for broad area fat reduction |
| LIPOVELA-V (Face) | Jawline, Double Chin | PPC, Deoxycholate, Peptides, Growth Factors | 2-4ml per facial area | Formulated for facial contouring and skin tightening |
Package Configuration
10ml × 10 Vials per Box
Formulation Type
Ready-to-Use Liquid Solution
Storage Temperature
Room Temperature (Below 30°C)
Post-Opening Storage
Refrigerated 5-10°C, Use within 7 days
LIPOVELA products are supplied as pre-mixed solutions in sterile vials, eliminating the need for complex preparation procedures. The formulation remains stable at room temperature for extended periods, with specific refrigeration requirements only after vial puncture to maintain potency and sterility.
05
Safety Information & Precautions
Important Safety Guidelines
Professional use only. Do not use in patients with known soy allergies. Contraindicated during pregnancy and breastfeeding. Avoid treatment below the knees where nerves are densely concentrated. Patients should avoid hot tubs, saunas, and strenuous exercise for several days post-treatment.
Prior to treatment, conduct thorough patient screening including allergy history, medical conditions, and current medications. Ensure proper injection technique to avoid vascular complications. Monitor patients for immediate adverse reactions and provide comprehensive post-treatment care instructions including adequate hydration recommendations.
-
!Contraindicated in patients with soybean allergies due to phosphatidylcholine content
-
!Not recommended for pregnant or nursing women due to safety considerations
-
!Avoid injection sites below the knee to prevent nerve damage risks
-
!Post-treatment restrictions include avoiding heat exposure and massage for 24-48 hours
Safety Protocol and Contraindication Guidelines
06
Frequently Asked Questions
How does LIPOVELA work to eliminate fat cells? ▼
LIPOVELA uses a dual-action mechanism combining sodium deoxycholate and phosphatidylcholine. Sodium deoxycholate acts as a detergent to destroy fat cell membranes, while PPC penetrates and dissolves the fat cells. L-Carnitine and B vitamins then accelerate the metabolic breakdown and elimination of released fatty acids through the body's natural processes.
What is the difference between LIPOVELA and LIPOVELA-V? ▼
LIPOVELA is designed for body areas like abdomen, thighs, and arms with higher volume capabilities (up to 10ml per site). LIPOVELA-V is specifically formulated for facial contouring with growth factors (EGF, FGF, IGF) and peptides for additional skin tightening benefits, using smaller volumes (2-4ml per area) suitable for delicate facial tissues.
How many treatment sessions are typically required? ▼
Body treatments typically require 2-3 sessions spaced 15 days apart for optimal results. Facial treatments with LIPOVELA-V generally need 2-4 sessions with 4-6 week intervals. Individual results may vary based on treatment area, fat volume, and patient response. Full effects are usually visible 6-8 weeks after the final session.
What post-treatment care is recommended? ▼
Patients should drink plenty of water to support the elimination process, avoid massaging treated areas for 24-48 hours, and refrain from hot tubs, saunas, and strenuous exercise for several days. Mild swelling and tenderness are normal and typically resolve within a few days. Follow all specific post-care instructions provided by your practitioner.
Are there any contraindications or restrictions? ▼
LIPOVELA should not be used in patients with soybean allergies, pregnant or breastfeeding women, or in areas below the knees where nerve density is high. Patients with certain medical conditions or taking specific medications should consult with their healthcare provider. Professional assessment is essential before treatment initiation.
07
Storage & Handling Requirements
LIPOVELA products require specific storage conditions to maintain potency and safety. Unopened vials should be stored at room temperature below 30°C in a dry, dark environment. Once a vial is punctured, it must be refrigerated at 5-10°C and used within a maximum of 7 days to ensure sterility and effectiveness.
-
✓Store unopened vials at room temperature below 30°C in original packaging
-
✓Refrigerate punctured vials at 5-10°C and use within 7 days maximum
-
✓Protect from direct sunlight and extreme temperature fluctuations
-
✓Ensure sterile handling techniques during preparation and application
Proper Storage and Handling Guidelines Visual
LIPOVELA V (5mL × 10 Vials)
6100
$61.00
Unit price perLIPOVELA V (5mL × 10 Vials)
6100
$61.00
Unit price perLIPOLYTIC SOLUTION
LIPOVELA V
FACIAL & LOCALIZED FAT REDUCTION
V-LINE CONTOURING SOLUTION
WHY KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
[PRODUCT IMAGE PLACEHOLDER - LIPOVELA V VIAL]
PRECISION FAT REDUCTION FOR DEFINED FACIAL CONTOURS
Advanced lipolytic formula combining Deoxycholic Acid, PPC, and L-Carnitine for effective fat cell destruction and natural metabolism. Specialized for V-line definition, double chin reduction, and localized fat targeting with minimal swelling.
PRODUCT SPECIFICATIONS
PACKAGING & VOLUME
10ml per vial, packaged as 5 vials per box (10ml × 5 vials). Liquid ampoule formulation designed for professional injection use.
KEY ACTIVE INGREDIENTS
🔹 DEOXYCHOLIC ACID
Primary fat cell destruction agent that breaks down adipose cell membranes through lipolysis. Works synergistically with PPC for enhanced fat reduction results.
🔹 PHOSPHATIDYLCHOLINE (PPC)
Works in combination with Deoxycholic Acid to emulsify and break down fat cells, facilitating their removal through the body's natural metabolic processes.
🔹 L-CARNITINE
Essential for transporting liberated fatty acids to be metabolized and naturally excreted by the body. Enhances the fat-burning process after cell breakdown.
🔹 BOTANICAL EXTRACTS
Including Juglans Regia Seed and Fucus Vesiculosus extracts that contribute to skin tightening and reduction of post-treatment swelling.
[MECHANISM OF ACTION INFOGRAPHIC - PPC/DEOXYCHOLIC ACID PROCESS]
EXPECTED TREATMENT EFFECTS
✓ V-LINE FACIAL CONTOURING: Defines jawline and creates the desired V-shaped facial profile
✓ DOUBLE CHIN REDUCTION: Effectively targets and reduces submental fat accumulation
✓ LOCALIZED FAT TARGETING: Addresses small, stubborn fat pockets in facial and body areas
✓ SKIN ELASTICITY MAINTENANCE: Prevents sagging with supportive ingredients post-fat reduction
✓ SWELLING MINIMIZATION: Botanical components reduce post-treatment edema for faster recovery
[TREATMENT AREA FACIAL MAPPING & DOSAGE GUIDE]
USAGE PROTOCOL & TREATMENT GUIDE
PRIMARY TREATMENT AREAS
- Double chin (submental area)
- Jawline and jowls
- Cheeks
- Small localized body areas (armpit folds, knees)
RECOMMENDED TREATMENT CYCLE
Typically requires 3-6 sessions performed at 1-week intervals. The exact number of sessions depends on the treatment area and volume of fat to be reduced.
APPLICATION METHOD
Direct syringe injection into the subcutaneous fat layer using multiple injection points within the target zone. Injection depth and volume per point must be adjusted based on the area's characteristics.
IMPORTANT ADMINISTRATION NOTES
- Inject strictly into the subcutaneous fat layer only
- Improper injection into muscle or dermis may cause complications
- Use proper sterile techniques throughout the procedure
- Adjust dosage based on individual patient needs and treatment area
TREATMENT STRATEGIES BY AREA
| TREATMENT STRATEGY | KEY INGREDIENT | TARGET AREA | TYPICAL DOSE PER SESSION | NOTABLE FEATURES |
|---|---|---|---|---|
| Facial Contouring | Deoxycholic Acid, PPC, L-Carnitine | Chin, Jawline, Cheeks | 4-8 ml (total) | Highly effective for defining V-line and removing double chin fat |
| Small Body Areas | Deoxycholic Acid, PPC, L-Carnitine | Axillary folds, underarms, knees | 6-10 ml (total) | Targeted reduction for localized, small-volume body fat deposits |
DETAILED PRODUCT DESCRIPTION
INGREDIENT COMPOSITION
Features a potent blend of Deoxycholic Acid, Phosphatidylcholine, and L-Carnitine for dual-action fat reduction and metabolism. Also includes anti-swelling and skin-firming botanical extracts for comprehensive treatment benefits.
PRIMARY TARGET AREAS
Primarily focused on the face (double chin, jawline) but effective for small, localized body fat deposits in areas such as armpit folds and knees.
EFFICACY SUMMARY
Provides significant lipolysis to destroy fat cells, promotes metabolism and lymphatic circulation, and offers a contouring effect with reduced post-procedure swelling. The inclusion of Deoxycholic Acid ensures permanent fat cell destruction for long-lasting results.
ADMINISTRATION GUIDELINES
Injections should be administered into the subcutaneous fat layer at multiple points within the target zone. The injection depth and volume per point must be adjusted based on the area's characteristics and individual patient needs.
ADDITIONAL BENEFITS
LIPOVELA V is formulated to minimize pain and swelling often associated with lipolytic treatments, promoting faster recovery and improved patient satisfaction. The permanent destruction of fat cells provides long-lasting contouring results without the need for maintenance treatments.
PRECAUTIONS & STORAGE GUIDELINES
STORAGE CONDITIONS
Store unopened vials at room temperature (1°C to 30°C), away from direct sunlight. Once opened, any unused solution should be discarded immediately. Do not freeze or expose to extreme temperatures.
TREATMENT INTERVAL PRECAUTIONS
Adhere strictly to the 1-week minimum interval between sessions to allow the body adequate time to process broken-down fat cells and minimize the risk of adverse reactions.
INJECTION PROTOCOL
- Inject strictly into the subcutaneous fat layer only
- Improper injection (e.g., into muscle or dermis) can cause discomfort or complications
- Use proper sterile techniques throughout the procedure
- Ensure proper needle depth and angle for safe administration
POST-TREATMENT CARE INSTRUCTIONS
- Avoid heat exposure (saunas, hot baths) for several days post-treatment
- Refrain from strenuous exercise for 48-72 hours
- Gentle massage of treated area may help promote lymphatic drainage
- Apply cold compress if swelling occurs
- Stay well-hydrated to support fat metabolism
TECHNICAL SPECIFICATIONS
FORMULATION TYPE
Liquid Ampoule
VOLUME PER VIAL
10ml
VIALS PER BOX
5 vials
STORAGE TEMPERATURE
1°C - 30°C
TREATMENT INTERVAL
1 week minimum
TYPICAL SESSION COUNT
3-6 sessions
FREQUENTLY ASKED QUESTIONS
HOW DOES LIPOVELA V WORK TO REDUCE FAT?
LIPOVELA V contains Deoxycholic Acid and Phosphatidylcholine (PPC) that work synergistically to destroy fat cell membranes through lipolysis. Once the fat cells are broken down, L-Carnitine facilitates the transport and metabolism of liberated fatty acids, allowing them to be naturally processed and excreted by the body. This results in permanent fat cell destruction and long-lasting contouring results.
WHAT IS THE EXPECTED TIMELINE FOR VISIBLE RESULTS?
Initial results may be visible within 2-4 weeks after the first treatment as the body begins to metabolize destroyed fat cells. Progressive improvements occur with each session. Optimal results are typically achieved 4-6 weeks after completing the full treatment cycle (3-6 sessions). Individual results may vary based on the treatment area, volume of fat, and patient's metabolic rate.
ARE THERE ANY CONTRAINDICATIONS OR LIMITATIONS?
LIPOVELA V should not be used in patients with active infections in the treatment area, bleeding disorders, or allergies to any of the ingredients. Pregnant or breastfeeding women should avoid this treatment. Patients with severe liver or kidney disease should consult with a healthcare professional before treatment. Not recommended for large-volume fat reduction or as a substitute for weight loss.
WHAT ARE THE PROPER STORAGE REQUIREMENTS?
Store unopened vials at room temperature between 1°C to 30°C, away from direct sunlight and extreme temperatures. Do not freeze the product. Once a vial is opened, any unused solution should be discarded immediately to maintain sterility and efficacy. Keep out of reach of children and unauthorized personnel. Check expiration date before use.
HOW IS LIPOVELA V DIFFERENT FROM OTHER FAT REDUCTION PRODUCTS?
LIPOVELA V features a unique triple-action formula combining Deoxycholic Acid for fat cell destruction, PPC for emulsification, and L-Carnitine for enhanced metabolism. The addition of botanical extracts helps minimize swelling and maintain skin elasticity. This comprehensive formulation is specifically designed for facial contouring and small localized areas, offering permanent fat reduction with minimal downtime and reduced post-treatment discomfort compared to traditional lipolytic treatments.
WHAT SHOULD PATIENTS EXPECT DURING RECOVERY?
Patients may experience mild swelling, bruising, or tenderness in the treated area for 3-7 days post-treatment. These effects are normal and indicate the product is working. Cold compresses can help reduce swelling. Most patients can return to normal activities within 24-48 hours, though strenuous exercise and heat exposure should be avoided for several days. Gentle massage of the treated area may promote lymphatic drainage and faster recovery.
PRODUCT KEYWORDS
PPC LIPOLYSIS DEOXYCHOLIC ACID FACIAL FAT DISSOLVING V-LINE CONTOURING DOUBLE CHIN REMOVAL LOCALIZED FAT REDUCTION L-CARNITINE SLIMMING LIPOLYTIC AMPOULE GENUINE DERMA PRODUCT
[PRODUCT PACKAGING AND SPECIFICATIONS PLACEHOLDER]
LIZTOX 100 Units (1 Vial)
3600
$36.00
Unit price perLIZTOX 100 Units (1 Vial)
3600
$36.00
Unit price perHUONS BIOPHARMA
Premium Botulinum Toxin Solutions
LIZTOX™ Injection
100 Units per Vial
[LIZTOX 100 Unit Product Image - Professional Vial Photography]
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Botulinum Toxin Type A
100 Units
Medical Grade
LIZTOX™ (Clostridium Botulinum Toxin Type A) 100 Units is a premium botulinum toxin solution designed for professional medical and aesthetic applications. This high-purity formulation (99.8% purity) provides exceptional results for treating moderate to severe facial wrinkles and various therapeutic conditions with minimal risk of resistance.
High Purity 99.8% - Fast Acting Formula
Key Components
1
Clostridium Botulinum Toxin Type A
Active Ingredient
100 Units
Primary Component
The main active ingredient responsible for muscle relaxation and wrinkle reduction. Highly purified at 99.8% purity for consistent results and minimal resistance risk.
2
Albumin
Stabilizing Agent
Trace Amount
Stabilizer
Provides stability to the toxin during storage and helps maintain protein integrity throughout the product's shelf life.
3
Sodium Chloride
Osmotic Agent
Isotonic Solution
Buffering Agent
Maintains proper osmotic balance and ensures comfortable injection with minimal tissue irritation.
[Molecular Structure Diagram - Botulinum Toxin Type A Composition]
Key Benefits & Applications
1
Glabellar Lines Treatment
Temporary improvement of moderate to severe frown lines between the eyebrows
with visible results in 3 days and peak effects in 1–2 weeks.
2
Crow's Feet Reduction
Effective treatment for lateral canthal lines (crow's feet) around the eyes, providing smoother appearance and improved facial aesthetics.
3
Forehead & Facial Lines
Relaxation of muscle contractions helping improve forehead lines, nasolabial folds, neck wrinkles, and masseteric hypertrophy.
4
Post-Stroke Spasticity Treatment
Therapeutic application for post-stroke upper limb spasticity, providing improved muscle function and patient comfort.
5
Extended Duration Results
Results typically last 3-4 months, with some cases extending up to 8 months, providing excellent value and patient satisfaction.
[Before & After Treatment Comparison - Facial Wrinkle Reduction Results]
Professional results with minimal downtime and high patient satisfaction rates
Professional Usage Protocol
1
Preparation & Reconstitution
Reconstitute the 100-unit vial with 2.5 mL of sterile, preservative-free 0.9% sodium chloride to achieve a concentration of 4 Units/0.1 mL. Gently swirl to dissolve - do not shake vigorously.
2
Dosage Determination
Calculate precise dosage based on treatment area: Glabellar Lines (20 units in five injection points), Crow's Feet (24 units total - 12 units per eye), Masseter Muscles (varies by individual).
3
Administration
Inject using appropriate technique for target area. Use sterile injection practices and proper needle selection for optimal results.
4
Post-Treatment Care
Use reconstituted solution within 24 hours. Monitor for immediate reactions and schedule follow-up as needed.
[Professional Injection Technique Guide - Step by Step Visual Instructions]
Treatment Timeline
Onset is typically observed around 3 days, with peak effects occurring within 1-2 weeks post-treatment. Results generally last 3-4 months, with some cases extending up to 8 months.
Product Specification Guide
| Volume | Main Use | Risk of Resistance | Duration | Treatment Area |
|---|---|---|---|---|
| 100U | Facial aesthetic procedures | Low (due to high purity) | 3-4 months | Glabella, crow's feet, forehead lines, minor areas |
The 100U vial is ideal for face-centric treatments, generally sufficient for procedures involving facial muscles with precise formulation for controlled injections.
Storage & Handling Specifications
| Parameter | Requirement | Notes |
|---|---|---|
| Storage Temperature | 2-8°C | Refrigerated storage required |
| Reconstitution | 2.5ml 0.9% Saline | Gently swirl, do not shake |
| Use After Reconstitution | Within 24 hours | Keep refrigerated after mixing |
| Package Contents | 1 Vial - 100 Units | Lyophilized powder |
| Purity Level | 99.8% | High purity formulation |
Important Handling Notes
- Do not use if vacuum seal on the vial is compromised upon opening
- The product comes as a lyophilized powder in a colorless, transparent vial
- Avoid vigorous shaking during reconstitution to prevent protein denaturation
- Use sterile technique throughout preparation and administration
- Intended for professional use only by trained medical professionals
Professional Use Only
This product is intended for use only by certified medical professionals. Consult a healthcare provider before use if you have neuromuscular disorders, are pregnant or breastfeeding, or are allergic to any ingredients.
Safety Information & Precautions
General Precautions
- Only for use by qualified medical professionals
- Proper patient assessment required before treatment
- Sterile injection technique must be maintained
- Monitor patients for adverse reactions
- Maintain proper cold chain storage at 2-8°C
Contraindications
- Pregnancy and breastfeeding
- Known allergies to botulinum toxin or albumin
- Neuromuscular disorders
- Active infection at injection site
- Avoid concurrent use of other botulinum toxin products
[Safety Guidelines Chart - Professional Administration Protocol]
Manufacturer Information
Huons Biopharma Co., Ltd.
Leading manufacturer of premium botulinum toxin products with advanced manufacturing facilities and strict quality control standards.
GMP Certified
ISO Compliant
Medical Grade
Quality Assurance
Each batch undergoes rigorous testing and quality control measures to ensure consistent potency, purity, and safety. The high-purity formulation (99.8%) helps minimize the risk of developing resistance or neutralizing antibodies.
Frequently Asked Questions
Q
What is LIZTOX 100 used for?
LIZTOX 100 is used for temporary improvement of moderate to severe glabellar (frown) lines, crow's feet, forehead and other facial lines, and as a therapeutic application for post-stroke upper limb spasticity.
Q
How soon does LIZTOX 100 work and how long do results last?
Onset is typically observed around 3 days, with peak effects within 1-2 weeks post-treatment. Results generally last 3-4 months, with some cases extending up to 8 months.
Q
What is the standard dilution for LIZTOX 100?
Reconstitute the 100-unit vial with 2.5 mL of sterile, preservative-free 0.9% sodium chloride to achieve a concentration of 4 Units/0.1 mL. Gently swirl to dissolve and do not shake vigorously.
Q
Who should administer LIZTOX 100?
LIZTOX 100 is intended for professional use only and should be administered exclusively by certified, trained medical professionals using sterile injection technique.
Q
Who manufactures LIZTOX?
LIZTOX is manufactured by Huons Biopharma Co., Ltd. in South Korea.
LIZTOX 200 Units (1 Vial)
5200
$52.00
Unit price perLIZTOX 200 Units (1 Vial)
5200
$52.00
Unit price perHUONS BIOPHARMA
Premium Botulinum Toxin Solutions
LIZTOX Injection
200 Units per Vial
[LIZTOX 200 Unit Product Image - Professional Vial Photography]
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Botulinum Toxin Type A 200 Units Medical Grade
LIZTOX Injection 200 Units is a premium botulinum toxin type A solution designed for professional medical and aesthetic applications. This high-purity formulation provides exceptional results for treating moderate to severe facial wrinkles, hyperhidrosis, and various muscular conditions.
High Purity 99.8% - Fast Acting Formula
Key Components
1
Clostridium Botulinum Toxin Type A
Active Ingredient
200 Units
Primary Component
The main active ingredient responsible for muscle relaxation and wrinkle reduction. Highly purified and standardized for consistent results.
2
Human Serum Albumin
Stabilizing Agent
Trace Amount
Stabilizer
Provides stability to the toxin during storage and helps maintain protein integrity throughout the product's shelf life.
3
Sodium Chloride
Osmotic Agent
Isotonic Solution
Buffering Agent
Maintains proper osmotic balance and ensures comfortable injection with minimal tissue irritation.
[Molecular Structure Diagram - Botulinum Toxin Type A Composition]
Key Benefits & Applications
1
Facial Wrinkle Treatment
Effectively treats moderate to severe glabellar lines, forehead wrinkles, and crow's feet with visible results in 3-7 days.
2
Hyperhidrosis Treatment
Provides effective treatment for excessive sweating in palms, armpits, and other affected areas with long-lasting results.
3
Blepharospasm Correction
Specialized treatment for involuntary eyelid spasms and related muscular conditions with precise dosing control.
4
Extended Duration
Results typically last 3-4 months, with some cases extending up to 6 months, providing excellent value and patient satisfaction.
[Before & After Treatment Comparison - Facial Wrinkle Reduction Results]
Professional results with minimal downtime and high patient satisfaction rates
Professional Usage Protocol
1
Preparation & Reconstitution
Dilute the 200-unit vial with 5 ml of 0.9% sterile saline. Gently swirl to dissolve the powder - do not shake vigorously to prevent denaturation.
2
Dosage Determination
Calculate precise dosage based on treatment area and individual patient needs. Consult dosage guidelines for specific applications.
3
Administration
Inject using appropriate technique for target area. Use sterile injection practices and proper needle selection for optimal results.
4
Post-Treatment Care
Provide patient with appropriate aftercare instructions. Monitor for immediate reactions and schedule follow-up as needed.
[Professional Injection Technique Guide - Step by Step Visual Instructions]
Treatment Timeline
Effects typically become visible within 3-7 days post-treatment, with maximum effect appearing within 1-2 weeks. Results generally last 3-4 months, with some cases extending up to 6 months.
Product Comparison Guide
| Volume | Main Use | Risk of Resistance | Duration | Treatment Area |
|---|---|---|---|---|
| 100U | Facial cosmetic procedures | Low | 3-4 months | Glabellar lines, crow's feet, forehead |
| 200U | Combined facial + body treatments | Low | 3-5 months | Glabellar lines, forehead, hyperhidrosis, calves |
The 200U version offers greater versatility for comprehensive treatment plans and multiple application areas in a single session.
Storage & Handling Specifications
| Parameter | Requirement | Notes |
|---|---|---|
| Storage Temperature | 2-8°C | Refrigerated storage required |
| Reconstitution | 5ml 0.9% Saline | Gently swirl, do not shake |
| Use After Reconstitution | Within 24 hours | Keep refrigerated at 2-8°C after mixing |
| Package Contents | 1 Vial - 200 Units | Single use vial |
| Shelf Life | As per package labeling | Check expiration date |
Important Handling Notes
- The vial may appear empty but contains lyophilized powder under pressure
- Avoid vigorous shaking during reconstitution to prevent protein denaturation
- Use sterile technique throughout preparation and administration
- Intended for professional use only by trained medical professionals
Professional Use Only
This product is intended for use only by trained and certified medical professionals. It has contraindications and potential side effects that must be discussed with a specialist before use.
Safety Information & Precautions
General Precautions
- Only for use by qualified medical professionals
- Proper patient assessment required before treatment
- Sterile injection technique must be maintained
- Monitor patients for adverse reactions
- Maintain proper cold chain storage
Contraindications
- Pregnancy and breastfeeding
- Known allergies to botulinum toxin or albumin
- Neuromuscular disorders
- Active infection at injection site
- Certain medications that affect neuromuscular transmission
[Safety Guidelines Chart - Professional Administration Protocol]
Manufacturer Information
Huons Biopharma Co., Ltd.
Leading manufacturer of premium botulinum toxin products with advanced manufacturing facilities and strict quality control standards.
GMP Certified ISO Compliant FDA Registered
Quality Assurance
Each batch undergoes rigorous testing and quality control measures to ensure consistent potency, purity, and safety. Complete batch tracking and documentation available for regulatory compliance.
Frequently Asked Questions
Q
What is LIZTOX 200 used for?
LIZTOX 200 is used to treat moderate to severe facial wrinkles (glabellar lines, forehead wrinkles, and crow's feet), hyperhidrosis (excessive sweating), and blepharospasm (involuntary eyelid spasms) and related muscular conditions.
Q
How soon does LIZTOX 200 work and how long do results last?
Effects typically become visible within 3-7 days post-treatment, with maximum effect appearing within 1-2 weeks. Results generally last 3-4 months, with some cases extending up to 6 months.
Q
What is the standard dilution for LIZTOX 200?
Dilute the 200-unit vial with 5 ml of 0.9% sterile saline. Gently swirl to dissolve the powder and do not shake vigorously to prevent denaturation.
Q
Who should administer LIZTOX 200?
LIZTOX 200 is intended for use only by trained and certified medical professionals, using sterile injection technique and proper patient assessment.
Q
Who manufactures LIZTOX?
LIZTOX is manufactured by Huons Biopharma Co., Ltd. in South Korea.
LusciLIPO (10mL × 5 Vials)
6400
$64.00
Unit price perLusciLIPO (10mL × 5 Vials)
6400
$64.00
Unit price per
LIPOLYTIC SOLUTION
LusciLipo
Lipolytic Solution
Advanced Fat Dissolving Formula with Bromelain
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Non-Surgical Fat Reduction Solution
Professional lipolytic formula combining Lecithin and Bromelain for effective fat reduction with minimized inflammation and swelling. Suitable for both facial and body contouring procedures.
Product Overview
Product Specifications
Product Name: LusciLIPO Lipolytic Solution
Formula Type: Single Formula (Face and Body Contouring)
Packaging: 10mL × 5 vials
Solution Type: Clear Injectable Solution
Formula Type: Single Formula (Face and Body Contouring)
Packaging: 10mL × 5 vials
Solution Type: Clear Injectable Solution
Key Ingredients & Mechanism
Core Active Ingredients
- Lecithin: Acts similarly to Phosphatidylcholine (PPC) by emulsifying and breaking down fat cells (adipocytes), promoting fat metabolism
- Bromelain: Natural enzyme with strong anti-inflammatory and anti-edema properties, minimizing post-treatment swelling and bruising
- Vitamin Complex (B Complex): Supports cellular metabolism and skin revitalization during the fat reduction process
- Natural Extracts: Enhances microcirculation and assists in detoxification through the lymphatic system
How It Works
LusciLIPO promotes fat reduction by utilizing Lecithin to induce the breakdown and dissolution of fat cells. The released lipids are metabolized and cleared from the body primarily via the lymphatic system. Bromelain plays a crucial role by reducing local inflammation and swelling, which improves the overall contouring process and accelerates recovery time.
Expected Results
Key Benefits
- Targeted Fat Reduction: Effectively reduces localized fat deposits in specific areas including double chin, jowls, abdomen, and thighs
- Improved Contours: Enhances facial definition (V-Line effect) and body contours for a more sculpted appearance
- Cellulite Reduction: Breaks down fat nodules associated with cellulite, promoting smoother skin texture
- Skin Firmness: Supports skin tightening effects post-fat reduction, contributing to improved skin elasticity and a more toned appearance
Usage Protocol & Treatment Guide
Treatment Areas
Facial Areas:
- Double chin (submental fat)
- Jawline (jowls)
- Chubby cheeks
Body Areas:
- Abdomen
- Flanks (love handles)
- Inner and outer thighs
- Buttocks
- Arms (bingo wings)
- Back fat
Recommended Treatment Cycle
A series of 3-6 sessions is typically recommended, with an interval of 1 to 2 weeks between each session. Visible results often become apparent after the 2nd or 3rd session as the body progressively metabolizes the dissolved fat.
Application Method
Localized injection into the subcutaneous fat layer using a sterile syringe (27G or 30G needle recommended). Inject small, consistent amounts (0.2-0.3 ml) per injection point, maintaining approximately 1 cm spacing between injection sites. Do not exceed recommended volume limits per session.
Treatment Strategy Guide
| Treatment Strategy | Key Focus | Target Area | Typical Dose | Notable Features |
|---|---|---|---|---|
| Facial Contouring | Lecithin, Bromelain | Chin, Jawline, Cheeks | 5-15ml total | Focused on V-line definition and swelling control |
| Broad Body Slimming | Lecithin, Vitamins | Abdomen, Thighs, Arms | 20-50ml total | Targets broader fat deposits and cellulite reduction |
The single LusciLipo formulation can be strategically applied across different body areas with adjusted dosing protocols. The presence of Bromelain provides a significant advantage in managing post-injection inflammation, making it suitable for both delicate facial areas and larger body zones.
Detailed Product Information
LusciLipo - Advanced Lipolytic Formula
Ingredient Composition: Lecithin, Bromelain, Vitamin complex, and beneficial Natural Extracts working synergistically for optimal results.
Ideal Target Areas: Effective for areas with excess fat accumulation and poor circulation, including facial zones (double chin) and various body areas requiring contouring.
Efficacy Summary: Promotes lipolysis (fat cell breakdown) combined with significant anti-inflammatory action and edema reduction due to Bromelain, leading to smoother contouring results and faster recovery time.
Application Technique: Requires precise injection into the targeted subcutaneous fat layer. Inject small, consistent amounts (0.2-0.3 ml per point), maintaining approximately 1 cm spacing between injection sites. Total volume per session should not exceed recommended safety limits.
Key Advantages
- Non-Surgical Option: Provides a minimally invasive approach to achieving body contouring goals without general anesthesia or surgical procedures
- Bromelain Advantage: The inclusion of Bromelain is a distinguishing feature, actively managing post-injection inflammation and promoting quicker return to daily activities
- Versatile Application: Single formula suitable for both facial and body treatments, offering flexibility in treatment planning
Precautions & Storage Guidelines
Storage Conditions
Store unopened vials in a cool, dry place away from direct sunlight. Recommended storage temperature: 1°C to 30°C. Once opened, handle remaining solution according to professional guidelines or discard appropriately. Do not freeze or expose to extreme temperatures.
Treatment Interval Guidelines
Maintain the recommended 7-to-14-day interval between sessions in the same treatment area. This allows sufficient time for the body to metabolize and clear the broken-down fat through the lymphatic system and enables proper healing of injection sites.
Post-Treatment Care
- Perform gentle massage on the treated area to promote even distribution and lymphatic drainage
- Maintain adequate hydration (increase water intake) to assist the body's natural detoxification processes
- Avoid strenuous exercise for 24-48 hours post-treatment
- Avoid alcohol consumption for 24 hours after treatment
- Apply cold compress if swelling occurs (Bromelain already minimizes this effect)
- Monitor treated areas for any unusual reactions and consult healthcare provider if concerns arise
Important Safety Information
This product is intended for professional use only. Treatments should be performed by qualified healthcare professionals trained in injection techniques. Not recommended for pregnant or nursing women, individuals with active infections at treatment sites, or those with known allergies to any ingredients. Consult with a healthcare provider before treatment if you have any medical conditions or concerns.
Technical Specifications
Package Size
10ml × 5 vials
Solution Type
Clear Injectable
Storage Temperature
1°C - 30°C
Application Area
Face & Body
Recommended Sessions
3-6 Sessions
Session Interval
1-2 Weeks
Frequently Asked Questions
How does LusciLipo differ from other fat dissolving injections?
LusciLipo features a unique combination of Lecithin for fat dissolution and Bromelain for anti-inflammatory effects. The inclusion of Bromelain is a key differentiator, as it actively manages post-injection inflammation and swelling, resulting in reduced downtime and improved patient comfort compared to standard fat dissolving solutions.
When can I expect to see results?
Visible results typically become apparent after the 2nd or 3rd treatment session, as the body progressively metabolizes the dissolved fat through the lymphatic system. Full results are usually achieved within 4-8 weeks after completing the recommended 3-6 session series, though individual response times may vary based on treatment area, metabolism, and lifestyle factors.
Is the treatment painful?
Discomfort during treatment is typically minimal to moderate and varies by individual pain tolerance and treatment area. Most patients describe a burning or stinging sensation during injection that subsides within minutes. Topical anesthetic can be applied before treatment to enhance comfort. The Bromelain component helps reduce post-treatment discomfort and swelling.
Are the results permanent?
When fat cells are broken down and eliminated through LusciLipo treatment, they do not regenerate. However, maintaining results requires a healthy lifestyle with proper diet and exercise. Significant weight gain after treatment can cause remaining fat cells to enlarge, potentially diminishing the contouring effects achieved.
What are the common side effects?
Common side effects include temporary swelling, redness, bruising, and tenderness at injection sites. These typically resolve within 3-7 days. The Bromelain component in LusciLipo is specifically included to minimize these effects. Rare side effects may include temporary numbness, itching, or firmness in treated areas. Serious adverse reactions are uncommon when administered by qualified professionals.
Who should not use LusciLipo?
LusciLipo is not recommended for pregnant or nursing women, individuals with active infections or inflammation at treatment sites, those with known allergies to any ingredients (especially bromelain or pineapple), people with severe liver or kidney disease, or those with bleeding disorders. A thorough consultation with a qualified healthcare provider is essential to determine treatment suitability.
LusciLIPO Orange (10mL × 5 Vials)
6200
$62.00
Unit price perLusciLIPO Orange (10mL × 5 Vials)
6200
$62.00
Unit price per
Luscilipo Orange
Professional Lipolytic Fat Dissolving Injection
Luscilipo Orange
10mL x 5 Vials
Advanced Fat Reduction & Body Contouring Solution
Premium lipolytic injection for targeted fat reduction in face and body areas
Lipolytic Injection
Body Contouring
Face Slimming
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Precision
Targeted fat reduction technology
Advanced formulation designed for precise targeting of localized fat deposits in both facial and body areas
Innovation
Scientific lipolysis breakthrough
Synergistic blend of natural extracts and vitamins for enhanced fat cell breakdown and skin firming
Safety
Natural ingredient formulation
Carefully selected natural extracts and vitamins with anti-inflammatory properties for safer treatment
Key Ingredients & Active Components
Bromelain
Active Enzyme
Powerful proteolytic enzyme that breaks down proteins and promotes fat cell dissolution. Known for its anti-inflammatory properties and ability to enhance lymphatic drainage.
Lecithin
Phospholipid Complex
Essential phospholipid that facilitates fat emulsification and cellular membrane breakdown. Acts as a natural lipolytic agent for effective fat reduction.
Vitamin Complex (B12, B2, C)
Essential Vitamins
Synergistic vitamin blend that supports cellular metabolism, enhances fat burning processes, and provides antioxidant protection for skin health.
Panax Ginseng Berry Extract
Premium Extract
Powerful adaptogenic extract that boosts circulation, enhances metabolic function, and provides energy support during the fat reduction process.
Centella Asiatica Extract
Healing Extract
Renowned for its healing and anti-inflammatory properties. Promotes collagen synthesis and helps maintain skin elasticity during fat reduction.
Expected Results & Benefits
Facial Contouring
-
V-Line DefinitionCreates defined jawline contours for a more sculpted facial appearance
-
Double Chin ReductionEffectively reduces submental fat for improved facial contour and a more refined jawline.
Body Contouring
-
Localized Fat ReductionTargets stubborn, localized fat deposits across body areas for a smoother, more contoured shape.
-
Cellulite ImprovementHelps reduce the appearance of cellulite while supporting skin firmness and elasticity.
Professional Use & Safety Information
Important Safety Information
This product is intended for administration by trained medical professionals only, who are knowledgeable in injection technique and anatomy.
- Not for use in pregnant or breastfeeding individuals.
- Avoid use in patients with known hypersensitivity to any component.
- Individual results and the number of recommended sessions vary by patient and treatment area.
- A qualified professional should assess suitability before treatment.
LUTHIONE Inj 600mg (10 Vials)
4700
$47.00
Unit price perLUTHIONE Inj 600mg (10 Vials)
4700
$47.00
Unit price per
Glutathione Injection
Daehan New Pharm
Antioxidant Therapy
Master Antioxidant for Skin & Health
LUTHIONE injection 600mg
Reduced Glutathione 600mg (10 Vials)
Professional-grade antioxidant injection for skin brightening, detoxification, and overall vitality enhancement
#SkinBrightening
#IVTherapy
#Detoxification
#AntiAging
Insert main product image: LUTHIONE injection 600mg packaging and vials
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Active Ingredients & Formulation
Each vial contains pharmaceutical-grade reduced glutathione in powder form for injection, ensuring maximum potency and stability.
Reduced Glutathione
Master antioxidant that protects cells from oxidative stress and supports cellular health
600mg per vial
Insert image: Glutathione molecular structure and mechanism of action infographic
Mechanism of Action
Glutathione works as a powerful antioxidant by neutralizing free radicals and protecting cells from oxidative damage. In skin lightening applications, it inhibits tyrosinase enzyme activity, promoting the synthesis of lighter pheomelanin over darker eumelanin. Additionally, it supports liver detoxification by binding to toxins and enhancing their excretion.
Antioxidant Action
Neutralizes free radicals and prevents cellular oxidative damage
Melanin Regulation
Inhibits tyrosinase enzyme and promotes lighter melanin production
Detoxification
Binds toxins and enhances liver detoxification processes
💡 Expected Benefits & Effects
Skin Brightening & Lightening
Promotes even skin tone and natural radiance through melanin regulation
Antioxidant Protection
Shields cells from free radical damage and oxidative stress
Anti-Aging Properties
Supports cellular health and may help reduce signs of aging
Detoxification Support
Enhances liver function and toxin elimination processes
Enhanced Immunity
Supports overall immune system function and vitality
Cellular Protection
Skin Enhancement
Liver Support
Vitality Boost
Key Benefits Summary
- Supports natural skin brightening through tyrosinase inhibition
- Provides powerful antioxidant protection against cellular damage
- Enhances liver detoxification and toxin elimination
- May contribute to anti-aging effects through cellular support
- Supports overall immunity and energy levels
Results may vary based on individual metabolism, consistent use, and overall health status. Optimal effects are typically observed with regular treatment protocols.
🧪 Professional Administration Protocol
1
Preparation
Reconstitute lyophilized powder with sterile water or appropriate solvent under sterile conditions
Reconstitute lyophilized powder with sterile water or appropriate solvent under sterile conditions
2
Dilution (for IV)
For intravenous administration, dilute in normal saline solution as per clinical protocol
For intravenous administration, dilute in normal saline solution as per clinical protocol
3
Administration
Administer via intramuscular (IM) or intravenous (IV) injection by qualified healthcare professional
Administer via intramuscular (IM) or intravenous (IV) injection by qualified healthcare professional
4
Monitoring
Monitor patient response and adjust treatment frequency based on individual needs
Monitor patient response and adjust treatment frequency based on individual needs
Recommended frequency: 1-2 times per week for initial course (5-10 sessions), followed by maintenance protocol (once every two weeks)
Combination Therapy Options
Enhanced Antioxidant Protocol
LUTHIONE injection 600mg is often combined with Vitamin C (Ascorbic Acid) injections to enhance antioxidant effects and improve glutathione absorption and regeneration.
- Vitamin C helps regenerate and prolong glutathione effects
- Thioctic Acid (Alpha-Lipoic Acid) may be added for comprehensive antioxidant coverage
- Combination therapy may provide enhanced skin brightening results
Insert image: Professional injection administration guide and combination therapy protocols
📊 Product Specifications
10
Vials per Package
600mg
Glutathione per Vial
Powder
Injection Form
Active Ingredient
Reduced Glutathione 600mg per vial
Package Contents
10 vials of lyophilized powder for injection
Administration
Intravenous (IV) or Intramuscular (IM) injection
Professional Use
Requires qualified healthcare professional administration
Manufacturer
Daehan New Pharm
⚠️ Important Safety Information
This product is for professional use only and must be administered by qualified healthcare professionals in appropriate clinical settings.
- Prescription required - not for self-administration
- Store at room temperature (1-30°C), before reconstitution
- Protect from direct sunlight and moisture
- Use immediately after reconstitution
- Keep out of reach of children
Contraindications and Precautions
- Do not use if pregnant or breastfeeding
- Contraindicated in patients with known allergies to glutathione
- Patients with cardiovascular conditions should consult physician
- Discontinue immediately if adverse reactions occur
- Not recommended for patients with certain medical histories
Emergency Response Protocols
- In case of allergic reaction: Discontinue immediately and seek medical attention
- For signs of anaphylaxis: Contact emergency services immediately
- Report any adverse effects to healthcare provider promptly
- Maintain emergency protocols in clinical setting during administration
❓ Frequently Asked Questions
A. LUTHIONE injection 600mg is used for skin brightening, antioxidant protection, detoxification support, and overall vitality enhancement through its reduced glutathione content. A. The active ingredient is Reduced Glutathione, 600mg per vial, a master antioxidant that protects cells from oxidative stress and supports cellular health. A. LUTHIONE is administered via intramuscular (IM) or intravenous (IV) injection after reconstituting the lyophilized powder. Typical frequency is 1-2 times per week for an initial course of 5-10 sessions, followed by maintenance every two weeks. A. LUTHIONE injections must be administered by qualified healthcare professionals. It is contraindicated during pregnancy, breastfeeding, and in patients with known glutathione allergies. A. LUTHIONE injection 600mg is manufactured by Daehan New Pharm under Good Manufacturing Practice (GMP) certified standards. A. LUTHIONE injections must be administered by qualified healthcare professionals, including licensed physicians, nurses, or trained medical practitioners in appropriate clinical settings with proper safety protocols. A. Typically 1-2 injections per week for an initial course of 5-10 sessions, followed by maintenance treatments every two weeks. The exact protocol should be determined by your healthcare provider based on individual needs. A. Yes, it's often combined with Vitamin C injections to enhance antioxidant effects. Thioctic Acid may also be included for comprehensive antioxidant therapy. Always consult with your healthcare provider about combination treatments. A. Store vials at room temperature (1-30°C), away from direct sunlight. Keep containers tightly sealed and use immediately after reconstitution. A. Effects may include skin brightening, enhanced antioxidant protection, improved detoxification, and increased vitality. Individual results vary based on metabolism and treatment consistency. Optimal effects typically observed with regular treatment protocols. A. While generally well-tolerated when administered properly, some individuals may experience allergic reactions. It's contraindicated during pregnancy, breastfeeding, and in patients with known glutathione allergies. Always consult healthcare providers before treatment.
Q. What is LUTHIONE injection 600mg used for?
Q. What is LUTHIONE's active ingredient?
Q. How is LUTHIONE administered?
Q. Who should administer LUTHIONE injections?
Q. Who is the manufacturer of LUTHIONE?
Q. Who can administer LUTHIONE injections?
Q. What is the recommended treatment protocol?
Q. Can LUTHIONE be combined with other treatments?
Q. How should the product be stored?
Q. What are the expected effects and timeline?
Q. Are there any side effects or contraindications?
📄 Clinical Guidelines & Documentation
Insert image: Professional clinical guidelines and administration protocols document
Professional Resources
Insert image: Dosage calculation chart and administration timeline guide
Insert image: Combination therapy protocols and compatibility chart
Clinical Manual
Comprehensive administration guidelines and safety protocols
Dosage Calculator
Professional dosing guidelines based on patient requirements
Compatibility Guide
Drug interaction and combination therapy reference
Training Materials
Educational resources for healthcare professionals
✅ Quality Assurance & Manufacturing Standards
GMP Certified
Pharmaceutical Grade
Quality Tested
Professional Use
Manufactured under strict pharmaceutical guidelines ensuring consistent quality, purity, and potency of each vial.
Manufacturing Excellence
Manufacturing
Good Manufacturing Practice (GMP) certified facility
Quality Control
Each batch tested for purity, potency, and sterility
Stability Testing
Rigorous stability studies ensuring product integrity
Regulatory Status
Complies with pharmaceutical regulations and standards
Traceability
Complete batch tracking and quality documentation
Insert image: Quality certification badges and manufacturing facility standards
🔬 Scientific Background & Research
Insert chart: Glutathione efficacy studies and clinical research data visualization
Glutathione Research Foundation
Glutathione has been extensively studied for its antioxidant properties, cellular protection mechanisms, and role in detoxification processes. Clinical research supports its use in various therapeutic applications including oxidative stress management and cellular health support.
600mg
Therapeutic Dose
IV/IM
Administration Routes
1-2x
Weekly Frequency
Research Focus
Antioxidant mechanisms and cellular protection studies
Clinical Applications
Oxidative stress management and wellness enhancement
Safety Profile
Well-established safety when administered by professionals
Luxfill (Fine / Deep / Sub-Q)
4100
$41.00
Unit price perLuxfill (Fine / Deep / Sub-Q)
4100
$41.00
Unit price perPremium Dermal Filler Collection
Luxfill
Fine / Deep / Sub-Q
Advanced hyaluronic acid dermal filler line designed for comprehensive facial rejuvenation and contouring with three specialized formulations
Hyaluronic Acid 24mg/ml Lidocaine 0.3% Non-Animal Origin
Three distinct formulations for comprehensive aesthetic applications from fine line correction to significant volume enhancement
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Active Ingredients & Technology
- Primary Active Complex
- Highly purified hyaluronic acid of non-animal origin utilizing advanced cross-linking technology for optimal biointegration and longevity.
Hyaluronic Acid 24mg/ml Lidocaine 0.3% Pre-filled Syringe 1.1mL
- h-DTP Cross-linking Technology
- Daejong Meditec's patented high-Density Tapping Process combines traditional and mechanical cross-linking with reduced BDDE agent for enhanced purity.
Monophasic Gel Structure High Purity Formula Reduced BDDE
-
Advanced Cross-linking
Patented h-DTP technology ensures optimal gel consistency and longevity while maintaining biocompatibility. -
Monophasic Structure
Smooth, consistent gel texture provides natural-looking results and improved injection experience. -
Enhanced Purity
Reduced cross-linking agents and advanced purification process minimize adverse reactions.
Clinical Benefits
- Corrects fine lines to deep wrinkles across multiple treatment areas
- Provides significant volume enhancement and facial contouring
- Delivers natural-looking results with improved skin elasticity
- Creates a subtle glowing effect through optimal tissue integration
- Long-lasting effects ranging from months to over a year
Natural Results Long-lasting Versatile
Clinical results demonstrate significant improvement in facial volume, wrinkle reduction, and overall skin quality across all treatment areas.
Product Specifications
| Product Version | Viscosity | Treatment Area | Injection Layer | Needle Gauge |
|---|---|---|---|---|
| Luxfill Fine | Low (100~200 pa-s) | Periorbital lines, lip contour, fine wrinkles | Superficial to mid-dermal | 30G |
| Luxfill Deep | Medium (200~300 pa-s) | Glabella, nasolabial folds, marionette lines | Mid to deep dermis | 27G |
| Luxfill Sub-q | High (300~500 pa-s) | Cheeks, jawline, chin, temples | Subcutaneous layer | 25G |
Standard Package Specifications
- Volume: 1.1 mL pre-filled syringe per package
- Concentration: Hyaluronic Acid 24mg/ml with Lidocaine 0.3%
- Gel Type: Monophasic structure for smooth injection
- Manufacturer: Daejong Meditec Co. Ltd.
Product Versions
Luxfill Fine
Efficacy
Corrects fine lines and wrinkles, plumps lip contours
Duration
Approximately 3-6 months
Treatment Area
Periorbital lines, fine mouth lines, lip contouring
Special Features
Lowest viscosity for delicate areas
Luxfill Deep
Efficacy
Corrects deep wrinkles, provides volumizing effects
Duration
Approximately 6-12 months
Treatment Area
Glabella lines, nasolabial folds, nose/forehead contour
Special Features
Medium viscosity for pronounced wrinkles
Luxfill Sub-q
Efficacy
Significant volumizing and contouring effects
Duration
Over 12 months (up to 24 months)
Treatment Area
Cheeks, jawline, chin, temples, body contouring
Special Features
Highest viscosity for structural support
Product Selection Guide
Which Luxfill is Right for You?
Choose the appropriate product based on treatment area and desired volume enhancement level.
Choose the appropriate product based on treatment area and desired volume enhancement level.
-
Natural Eye Area Improvement
Luxfill Fine - Ideal for delicate periorbital areas and subtle lip enhancement -
Moderate Wrinkle Correction
Luxfill Deep - Perfect for nasolabial folds and facial contouring -
Structural Volume Enhancement
Luxfill Sub-q - Best for significant cheek and jawline augmentation
Storage & Safety Information
Storage Requirements — Store at room temperature between 1°C and 30°C. Do not freeze or heat. Keep away from direct sunlight.
Professional Use Only — This product is intended for use by trained, qualified aesthetic professionals only.
-
Minimal Side Effects
High purity formulation reduces risk of swelling or redness -
Quality Assurance
Advanced purification process ensures consistent product quality -
Professional Training
Proper injection technique training recommended for optimal results
Frequently Asked Questions
What is Luxfill used for?
Luxfill is a hyaluronic acid dermal filler line used to correct fine lines to deep wrinkles, provide volume enhancement and facial contouring, and plump lip contours across periorbital lines, nasolabial folds, cheeks, jawline, chin, and temples depending on the formulation.
What is Luxfill made of?
Luxfill is made of highly purified hyaluronic acid of non-animal origin at 24mg/ml with 0.3% lidocaine, formulated as a monophasic gel using Daejong Meditec's patented h-DTP (high-Density Tapping Process) cross-linking technology with reduced BDDE.
How long do results from Luxfill last?
Duration depends on the formulation: Luxfill Fine lasts approximately 3-6 months, Luxfill Deep approximately 6-12 months, and Luxfill Sub-q over 12 months (up to 24 months).
Who should administer Luxfill?
Luxfill is intended for use by trained, qualified aesthetic professionals only. Proper injection technique training is recommended for optimal results.
Who manufactures Luxfill?
Luxfill is manufactured by Daejong Meditec Co. Ltd.
Mayfill Dermal Filler Series (Light / Deep / Volume)
4400
$44.00
Unit price perMayfill Dermal Filler Series (Light / Deep / Volume)
4400
$44.00
Unit price per
Mayfill Cross-linked HA 20mg/ml 0.3% Lidocaine
Mayfill Dermal Filler Series
Light / Deep / Volume
Advanced cross-linked hyaluronic acid dermal fillers with R2 Technology for comprehensive facial rejuvenation and contouring
Multi-layered Phasic structure with BDDE cross-linking - 2ml per package (1ml x 2 syringes)
[Main Product Image - Mayfill Series Three Versions]
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Professional-grade hyaluronic acid fillers with R2 Technology for natural results and excellent moldability
Package Contents
- 2 pre-filled syringes of 1ml each
- Cross-linked Hyaluronic Acid 20mg/ml
- 0.3% Lidocaine for comfortable treatment
- Available in three specialized versions
Key Technology
R2 Technology BDDE Cross-linking Multi-layered Phasic High Moldability
[R2 Technology Mechanism Diagram]
Composition & Technical Features
Active IngredientCross-linked Hyaluronic Acid (HA)
Concentration
20mg/ml
Anesthetic0.3% Lidocaine
Cross-linking MethodBDDE cross-linking with Multi-layered Phasic structure
Gel StructureMulti-layered Phasic gel type
Formulation TypeSyringe type, 1ml x 2 syringes per box
TechnologyR2 Technology (Rotation & Revolution) creates pure and uniform gel with high viscosity and excellent moldability
Product Variants Comparison
Choose a product with different viscosity and injection layers depending on the treatment area and soft tissue volume
| Product Name | Viscosity | Treatment Area | Injection Layer | Needle Gauge |
|---|---|---|---|---|
| Light | Low | Fine lines on forehead, eye area, glabella, perioral lines | Mid Dermis | 27G, 30G |
| Deep | Medium | Deep wrinkles, nasolabial folds, lips | Mid Dermis, Deep Dermis | 27G |
| Volume | High | Forehead, cheeks, chin, nose, jawline | Deep Dermis, Sub-Q | 25G, 27G |
[Treatment Areas Comparison - Before and After]
Mayfill Light
Light Fine Lines Delicate Areas
Primary Applications
Corrects fine lines and light wrinkles, especially in delicate areas. Its low viscosity makes it ideal for precise, superficial injections to smooth skin texture.
Forehead Lines Crow's Feet Perioral Wrinkles Glabellar Lines
Key Benefits
Duration
Approximately 6-8 months
Usage
Inject into the mid dermis with a 27G or 30G needle
- Low viscosity for precise injections
- Ideal for delicate facial areas
- Smooth skin texture enhancement
[Mayfill Light Treatment Results]
Mayfill Deep
Deep Deep Wrinkles Natural Volume
Primary Applications
Effectively improves moderate to deep wrinkles and provides natural-looking volume. The medium viscosity gel allows for versatile application.
Nasolabial Folds Marionette Lines Forehead Wrinkles Lip Enhancement
Key Benefits
Duration
Approximately 9-12 months
Usage
Inject into the mid to deep dermis with a 27G needle
- Medium viscosity for versatile application
- Both wrinkle correction and subtle volume
- Natural-looking results
[Mayfill Deep Before and After Comparison]
Mayfill Volume
Volume Facial Contouring Structural Enhancement
Primary Applications
Provides powerful volumizing and contouring for facial features. With the highest viscosity in the series, it is designed for structural enhancement and creating defined contours.
Cheeks Chin Nose Jawline
Key Benefits
Duration
Approximately 12+ months
Usage
Inject into the deep dermis or subcutaneous layer with a 25G or 27G needle
- Highest viscosity for structural support
- Powerful volumizing and contouring
- Long-lasting defined contours
[Mayfill Volume Facial Contouring Results]
Which Product Is Right for Me?
Choose a product with different viscosity and injection layers depending on the treatment area and soft tissue volume
Natural improvement of fine lines → Light
Choose Light for fine lines correction in delicate areas like forehead, eye area, and perioral regions
Light
Deep wrinkle correction → Deep
Choose Deep for moderate to deep wrinkles, nasolabial folds, and natural volume enhancement
Deep
Structural volume enhancement → Volume
Choose Volume for facial contouring, structural support, and powerful volumizing of cheeks, chin, nose, and jawline
Volume
Efficacy Benefits
Smoothing Fine Lines and Deep Wrinkles
Comprehensive wrinkle correction from fine lines to deep facial folds
Volume Enhancement
Restore lost facial volume in key facial areas for natural rejuvenation
Facial Contouring
Enhance facial contours and create defined structure with natural results
Treatment Guidelines
Recommended Treatment Cycle
Duration varies depending on the product version and patient's individual characteristics
Light Version
Approximately 6-8 months
Deep Version
Approximately 9-12 months
Volume Version
Approximately 12+ months
Professional Administration
- Inject into appropriate dermis layers based on product version
- Use recommended needle gauges for optimal results
- Follow proper injection techniques
- Professional use only
Safety Information & Storage
Important Precautions — Do not inject into blood vessels. Use with caution in patients with a history of severe allergies. Consult a qualified professional before use.
Storage Requirements
- Store at 2-30°C in a shaded area
- Keep away from direct sunlight
- Do not freeze
- Must be used immediately after opening
Safety Guidelines
- Professional administration required
- Check for hypersensitivity before treatment
- Do not use in patients with known HA allergies
- Follow sterile injection procedures
[Storage and Safety Instructions Infographic]
Frequently Asked Questions
- What is Mayfill used for?
- Mayfill is a cross-linked hyaluronic acid dermal filler series used for smoothing fine lines to deep wrinkles, volume enhancement, and facial contouring across areas such as the forehead, eye area, perioral lines, nasolabial folds, lips, cheeks, chin, nose, and jawline depending on the variant.
- What is Mayfill made of?
- Mayfill is made of cross-linked hyaluronic acid at 20mg/ml with 0.3% lidocaine, formulated as a multi-layered phasic gel using BDDE cross-linking and R2 Technology (Rotation & Revolution) for a pure, uniform gel with high viscosity and excellent moldability.
- How long do results from Mayfill last?
- Duration varies by version: Mayfill Light lasts approximately 6-8 months, Mayfill Deep approximately 9-12 months, and Mayfill Volume approximately 12+ months, depending on the product version and the patient's individual characteristics.
- Who should administer Mayfill?
- Mayfill is for professional use only and requires professional administration. Check for hypersensitivity before treatment, do not use in patients with known HA allergies, use with caution in patients with a history of severe allergies, and do not inject into blood vessels.
MELSMON Inj (2mL × 50 Amps)
41000
$410.00
Unit price perMELSMON Inj (2mL × 50 Amps)
41000
$410.00
Unit price perProfessional Injectable
MELSMON injection
2mL x 50 Ampoules
Advanced placenta extract formulation designed for skin regeneration and overall wellness enhancement
Why KSTATION
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
[MELSMON Product Package and Ampoule Photography]
Composition
Key Components
Human Placenta Extract
100mg per 2mL
Primary active component containing over 100 bioactive substances including amino acids, peptides, mucopolysaccharides, enzymes, minerals, and vitamins essential for cellular regeneration and tissue repair.
[Molecular Structure and Bioactive Components Infographic]
Amino Acids & Peptides
Complex
Essential building blocks for collagen and elastin synthesis, promoting natural tissue repair and cellular regeneration processes at the molecular level.
Vitamins & Minerals
Multi-complex
Comprehensive vitamin and mineral profile supporting metabolism enhancement, antioxidant protection, and overall cellular vitality maintenance.
Therapeutic Benefits
Main Expected Effects
1
Comprehensive Skin Regeneration
Enhanced skin elasticity, improved hydration levels, and reduction of fine lines, wrinkles, and hyperpigmentation through stimulated cellular regeneration processes.
2
Menopausal Symptom Relief
Significant alleviation of various menopausal symptoms including hot flashes, mood swings, fatigue, and sleep disturbances through natural hormonal balance support.
3
Enhanced Recovery & Vitality
Accelerated post-procedure recovery, improved stress resistance, and enhanced overall vitality through metabolic optimization and energy enhancement.
4
Natural Regenerative Therapy
Non-hormonal, natural-origin therapeutic approach that activates the body's own regenerative processes for comprehensive wellness improvement.
[Before & After Results and Clinical Benefits Visualization]
Administration
Professional Usage Protocol
1
Pre-Treatment Assessment
Comprehensive patient evaluation and treatment area assessment by qualified healthcare professional to determine optimal injection protocol and dosage requirements.
2
Professional Administration
Subcutaneous or intramuscular injection performed by trained medical professional using sterile technique and appropriate injection methodology for optimal results.
3
Treatment Schedule
Standard protocol involves 2-3 injections per week for 4-6 weeks, with maintenance sessions recommended every few months based on individual response and goals.
4
Progress Monitoring
Regular assessment of treatment response and adjustment of protocol as needed to ensure optimal therapeutic outcomes and patient satisfaction.
[Professional Administration Technique Guide and Injection Areas]
Treatment Protocols
Recommended Applications by Target
Skin Rejuvenation Protocol
For dull, sagging, or dry skin conditions with fine lines and hyperpigmentation. Stimulates cellular regeneration, collagen, and elastin synthesis to restore skin vitality and firmness.
Menopausal Support Protocol
Specialized treatment for hot flashes, mood swings, fatigue, and insomnia related to menopause. Supports hormonal balance and improves overall well-being through natural therapy.
Post-Procedure Recovery Protocol
Enhanced recovery support after cosmetic procedures, chemical peels, or surgeries. Accelerates tissue repair processes and reduces rehabilitation time significantly.
General Wellness Protocol
Comprehensive wellness support for chronic fatigue, low energy, and poor stress resistance. Rich blend of amino acids and vitamins improve metabolism and boost vitality.
[Treatment Protocol Infographic and Professional Guidelines]
| Specification | Details |
|---|---|
| Package Contents | 50 Ampoules × 2.0 mL each |
| Active Ingredient | Human Placenta Extract 100mg per ampoule |
| Administration Route | Subcutaneous or Intramuscular Injection |
| Storage Temperature | 1-30°C (Room Temperature) or 2-8°C (Refrigerated) |
| Treatment Duration | 4-6 weeks initial course |
| Professional Use | Qualified Healthcare Professional Required |
Important Safety Information
Professional use only. Not suitable for individuals with allergies to placenta-derived products. Generally avoided during pregnancy or breastfeeding. Store in hermetic container away from direct sunlight. Mild side effects such as redness or tenderness at injection site may occur. Users are generally restricted from donating blood due to theoretical risk of transmission. Always administered by qualified healthcare professional.
[Product Documentation, Regulatory Compliance, and Professional Guidelines]
Frequently Asked Questions
Frequently Asked Questions
What is MELSMON injection used for?
MELSMON injection is a human placenta extract therapy used for comprehensive skin regeneration (improved elasticity and hydration, reduction of fine lines, wrinkles, and hyperpigmentation), relief of menopausal symptoms such as hot flashes, mood swings, fatigue, and sleep disturbances, enhanced post-procedure recovery, and general wellness and vitality support.
What is MELSMON's active ingredient?
The active ingredient is Human Placenta Extract at 100mg per 2mL ampoule, containing over 100 bioactive substances including amino acids, peptides, mucopolysaccharides, enzymes, minerals, and vitamins essential for cellular regeneration and tissue repair.
How is MELSMON administered?
MELSMON is administered via subcutaneous or intramuscular injection by a qualified healthcare professional using sterile technique. The standard protocol involves 2-3 injections per week for 4-6 weeks, with maintenance sessions every few months based on individual response.
Who should administer MELSMON and what are the precautions?
MELSMON is for professional use only and must always be administered by a qualified healthcare professional. It is not suitable for individuals with allergies to placenta-derived products and is generally avoided during pregnancy or breastfeeding. Mild side effects such as redness or tenderness at the injection site may occur, and users are generally restricted from donating blood due to a theoretical risk of transmission.
MELSMON Excellence
MELSMON injection represents advanced placenta extract therapy with comprehensive regenerative benefits. This professional-grade treatment delivers consistent results through rigorously tested natural components, providing skin rejuvenation, menopausal support, and overall wellness enhancement backed by clinical research and quality assurance standards.
MENNUS (PLA 200mg × 1 Vial)
9900
$99.00
Unit price perMENNUS (PLA 200mg × 1 Vial)
9900
$99.00
Unit price perCOLLAGEN BIOSTIMULATOR
MENNUS
PLA 200mg x 1 Vial
ADVANCED NEOCOLLAGENESIS TECHNOLOGY
[MENNUS PRODUCT HERO IMAGE PLACEHOLDER]
WHY KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
LONG-LASTING COLLAGEN REGENERATION
Advanced biostimulator that promotes neocollagenesis for sustained facial volume restoration and wrinkle improvement through natural collagen production stimulation over an extended period.
ACTIVE INGREDIENTS & COMPOSITION
POLY-D,L-LACTIC ACID (PLA)
PRIMARY COMPONENT
Biodegradable spherical PLA particles that stimulate natural collagen synthesis through controlled tissue response. The spherical particle shape ensures even volume creation and prevents needle blockage during injection.
CARBOXYMETHYL CELLULOSE (CMC)
SECONDARY COMPONENT
CMC gel component provides immediate volumizing effect while serving as a carrier matrix for PLA particles, ensuring optimal distribution and biocompatibility.
TOTAL FORMULATION
200mg of combined PLA and CMC ingredients per vial in freeze-dried powder form. This biostimulator formulation is designed to restore and maintain facial volume by promoting the body's natural collagen production.
BIODEGRADABLE
SPHERICAL PARTICLES
FREEZE-DRIED TECHNOLOGY
[PLA MICROSPHERE MECHANISM VISUALIZATION PLACEHOLDER]
KEY BENEFITS & EFFECTS
01
LONG-LASTING COLLAGEN REGENERATION
Stimulates natural collagen synthesis for sustained improvement lasting 18-24 months with progressive tissue regeneration.
02
FACIAL VOLUME RESTORATION
Restores lost facial volume and contours through dual-action mechanism: immediate CMC gel effect and long-term PLA stimulation.
03
WRINKLE IMPROVEMENT
Effectively improves both fine and deep wrinkles through enhanced skin elasticity and firmness from collagen regeneration.
04
SKIN TEXTURE ENHANCEMENT
Improves overall skin texture, elasticity, and firmness through comprehensive neocollagenesis process.
DUAL-PHASE EFFECTIVENESS
- Immediate volume effect from CMC gel component lasting 3-9 months
- Secondary long-term effects from collagen regeneration lasting 6-24 months
- Total treatment efficacy extends up to 18-24 months
- Progressive improvement through natural collagen synthesis
[BEFORE/AFTER TREATMENT RESULTS PLACEHOLDER]
STEP-BY-STEP USAGE PROTOCOL
1
PREPARATION & RECONSTITUTION
Reconstitute the freeze-dried powder with sterile distilled water. Optional: mix with 1-2 mL of 2% Lidocaine for enhanced patient comfort during treatment.
2
NEEDLE PREPARATION
Use 18G needle to withdraw the reconstituted solution, then switch to 26G needle for precise injection into the targeted treatment area.
3
INJECTION TECHNIQUE
Inject into dermal layer or subcutaneous layer depending on treatment area. The spherical PLA particles ensure smooth injection with low pressure requirements.
4
TREATMENT AREAS
Apply to entire facial area excluding glabella and eye region. Suitable for deep forehead wrinkles, nasolabial folds, temporal and cheekbone augmentation.
5
POST-TREATMENT CARE
Monitor patient response and schedule follow-up treatments as needed. Treatment cycle consists of 1-3 sessions for optimal results.
TREATMENT FREQUENCY & TIMING
Recommended treatment cycle of 1-3 treatments. Single treatment session provides immediate volume for 3-9 months, with secondary efficacy from collagen regeneration lasting 6-24 months.
APPLICATION PROTOCOLS
INJECTION LAYER SPECIFICATIONS
Target dermal layer or subcutaneous layer based on treatment objectives. Deep dermis injection for wrinkle correction, subcutaneous for volume restoration.
NEEDLE GAUGE PROTOCOL
Use 18G needle for solution withdrawal to prevent particle damage, then 26G needle for patient injection to ensure comfort and precision.
[INJECTION TECHNIQUE REFERENCE GUIDE PLACEHOLDER]
PRODUCT SPECIFICATIONS
| SPECIFICATION | VALUE | DESCRIPTION |
|---|---|---|
| Total Volume | 200mg | Per single vial |
| Formulation Type | Freeze-dried powder | Lyophilized spherical particles |
| Cross-linking | Not cross-linked | Non-cross-linked gel structure |
| Particle Shape | Spherical | Even volume creation |
| Storage Temperature | 2-25°C | Room temperature storage |
| Shelf Life | 24 months | From manufacture date |
STORAGE & HANDLING CONDITIONS
Store at room temperature (2-25°C) away from direct sunlight. Keep in original packaging until use. For professional use only by certified medical professionals or dermatologists.
ROOM TEMPERATURE
LIGHT PROTECTION
PROFESSIONAL USE
TREATMENT DURATION & RESULTS
3-9
MONTHS
Initial volume effect duration
6-24
MONTHS
Secondary collagen effect
18-24
MONTHS
Total treatment efficacy
1-3
TREATMENTS
Recommended treatment cycle
200
MG
Active ingredient per vial
26G
NEEDLE
Recommended injection gauge
[TREATMENT TIMELINE AND RESULTS CHART PLACEHOLDER]
MANUFACTURER & QUALITY STANDARDS
MANUFACTURER INFORMATION
Manufactured by Maypharm Co., Ltd. utilizing advanced freeze-drying technology to reduce reconstitution time and ensure optimal particle integrity.
QUALITY FEATURES
- Spherical PLA particles for even distribution
- Low injection pressure requirements
- Biodegradable materials with no residue
- Freeze-drying technology for stability
- Professional-grade formulation standards
SAFETY INFORMATION & PRECAUTIONS
For professional use only by certified medical professionals or dermatologists. Read complete instructions before use.
- Professional administration required
- Avoid glabella and eye region
- Store away from direct sunlight
- Use proper needle gauge specifications
- Monitor patient response during treatment
- Follow recommended reconstitution procedures
- Maintain sterile injection techniques
- Document treatment parameters
PROFESSIONAL GUIDELINES
This product is intended for use by qualified medical professionals only. Proper training in injection techniques and facial anatomy is essential for safe and effective treatment outcomes.
TECHNICAL DOCUMENTATION
FORMULATION TECHNOLOGY
MENNUS utilizes advanced freeze-drying technology combined with spherical PLA particle engineering to ensure optimal biocompatibility and treatment effectiveness.
FREEZE-DRIED
SPHERICAL PARTICLES
BIOSTIMULATOR
MECHANISM OF ACTION
Dual-phase mechanism combining immediate volumizing from CMC gel with long-term collagen stimulation from PLA microspheres. The biodegradable components are naturally processed by the body, leaving enhanced tissue structure through neocollagenesis.
META KEYWORDS
Poly-L-Lactic Acid Filler, PLA Filler, CMC Filler, Collagen Stimulator, Neocollagenesis, Long-Lasting Filler, Facial Volume, Wrinkle Improvement, Injectable, Maypharm, Biodegradable Filler, Skin Rejuvenation
FREQUENTLY ASKED QUESTIONS
What is MENNUS used for?
MENNUS is a PLA collagen biostimulator used for long-lasting collagen regeneration, facial volume restoration, and improvement of both fine and deep wrinkles, as well as overall skin texture, elasticity, and firmness. It is suitable for the entire facial area excluding the glabella and eye region, including deep forehead wrinkles, nasolabial folds, temporal and cheekbone augmentation.
What is MENNUS's key ingredient?
MENNUS contains 200mg per vial of Poly-D,L-Lactic Acid (PLA) as biodegradable spherical particles that stimulate natural collagen synthesis, combined with Carboxymethyl Cellulose (CMC) gel that provides an immediate volumizing effect and acts as a carrier matrix.
How is MENNUS prepared?
The freeze-dried powder is reconstituted with sterile distilled water, optionally with 1-2 mL of 2% Lidocaine. An 18G needle is used to withdraw the solution, then a 26G needle is used to inject into the dermal or subcutaneous layer depending on the treatment area.
How long do results last?
The immediate volume effect from the CMC gel lasts 3-9 months, while collagen regeneration provides secondary effects lasting 6-24 months, for total treatment efficacy of up to 18-24 months. A cycle of 1-3 treatments is recommended.
Who should administer MENNUS?
MENNUS is for professional use only by certified medical professionals or dermatologists with proper training in injection techniques and facial anatomy. Sterile injection technique must be maintained and the glabella and eye region avoided.
Who manufactures MENNUS?
MENNUS is manufactured by Maypharm Co., Ltd., utilizing advanced freeze-drying technology to reduce reconstitution time and ensure optimal particle integrity.
[PRODUCT PACKAGING AND VIAL SPECIFICATIONS PLACEHOLDER]
MENNUS PLUS (PLA 360mg × 1 Vial)
8800
$88.00
Unit price perMENNUS PLUS (PLA 360mg × 1 Vial)
8800
$88.00
Unit price perPLLA Biostimulator
MENNUS PLUS
PLA 360mg x 1 Vial
Advanced poly-L-lactic acid (PLLA) based filler designed for long-lasting collagen synthesis and volume restoration
BIOSTIMULATOR
COLLAGEN BOOSTER
18-24 MONTHS
Single vial containing 360mg of poly-L-lactic acid powder for professional use
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Active Ingredients
- Primary Active Component
- Poly-L-lactic Acid (PLLA) - A biodegradable and biocompatible polymer that stimulates the body's natural collagen production.
- Reconstitution Components
- For preparation, mix with 8-10ml of sterile distilled water and 1-2ml of 2% Lidocaine for optimal injection experience.
PLA 360mg per vial
Biodegradable
Biocompatible
Sterile Water 8-10ml
2% Lidocaine 1-2ml
Freeze-dry Technology
-
Collagen Stimulation
PLLA particles encourage the body to produce its own collagen, leading to natural and gradual improvement over time. -
Spherical Design
Specially designed spherical PLA particles allow for easy injection without needle blockage and create even, stable volume. -
Fast Dilution
Freeze-drying technology enables faster reconstitution and smoother injection experience.
Clinical Benefits
- Long-lasting collagen regeneration and volume restoration
- Improvement of deep wrinkles and fine lines
- Overall skin rejuvenation and increased elasticity
- Natural and gradual improvement over 18-24 months
Volume Restoration
Wrinkle Improvement
Skin Elasticity
Initial volume effect lasts 3-9 months, while collagen regeneration provides lasting results for 18-24 months.
Treatment Protocol
Preparation
Reconstitute 360mg PLA powder with 8-10ml sterile distilled water and 1-2ml of 2% Lidocaine
Reconstitute 360mg PLA powder with 8-10ml sterile distilled water and 1-2ml of 2% Lidocaine
Withdrawal
Use 18G needle to withdraw the reconstituted solution from the vial
Use 18G needle to withdraw the reconstituted solution from the vial
Injection
Inject using 26G needle or 25G cannula into superficial dermal to subcutaneous layer
Inject using 26G needle or 25G cannula into superficial dermal to subcutaneous layer
Post-Treatment
Perform recommended massage and provide proper aftercare instructions to patients
Perform recommended massage and provide proper aftercare instructions to patients
Treatment Sessions
1-3 sessions depending on individual needs
Effect Duration
18-24 months for collagen regeneration
Injection Layer
Superficial dermal to subcutaneous
Treatment Applications
| Treatment Strategy | Viscosity | Treatment Area | Injection Layer | Needle Gauge |
|---|---|---|---|---|
| Facial Volume & Contouring | Medium | Cheeks, temporal area, nasolabial folds, chin | Dermal to subcutaneous | 25G cannula or 26G needle |
| Skin Rejuvenation | Low (after dilution) | Face, neck & decollete, hands | Superficial dermal | 26G needle |
Suitable Treatment Areas
- Face: cheeks, chin, temporal area, nasolabial folds
- Neck and decollete area for skin quality improvement
- Hands for volume restoration and skin rejuvenation
- Any area requiring long-term collagen stimulation
Storage & Safety Information
Storage Requirements
- Store at 2°C ~ 25°C in a cool, dry environment
- Protect from direct sunlight and extreme temperatures
- Use reconstituted product within 72 hours
- Keep vial tightly sealed when not in use
Important Precautions — Avoid use in patients with history of keloid formation or hypertrophic scarring. Common injection-related reactions may include swelling, pain, or hemorrhage.
Post-Treatment Care — Patients should avoid saunas, swimming pools, and vigorous exercise for at least one week. Proper massage technique should be performed as instructed.
Frequently Asked Questions
How does MENNUS PLUS differ from traditional fillers?
Unlike temporary fillers, MENNUS PLUS is a biostimulator that works by encouraging the body to produce its own collagen, leading to natural and gradual improvement that lasts 18-24 months.
What is the reconstitution process?
Mix the 360mg PLA powder with 8-10ml of sterile distilled water and 1-2ml of 2% Lidocaine. The freeze-drying technology allows for faster dilution and smoother injection.
How many treatment sessions are typically needed?
Generally 1-3 sessions are recommended depending on individual patient needs and desired outcomes. The treatment plan should be customized for each patient.
What are the expected results timeline?
Initial volume effect from the CMC gel component lasts approximately 3-9 months, while the secondary effect from collagen regeneration provides lasting results for 18-24 months.
Frequently Asked Questions
- What is MENNUS PLUS used for?
- MENNUS PLUS is a PLLA biostimulator filler used for long-lasting collagen regeneration and volume restoration, improvement of deep wrinkles and fine lines, and overall skin rejuvenation with increased elasticity. It is suitable for the cheeks, chin, temporal area, nasolabial folds, neck, decollete, and hands.
- What is MENNUS PLUS's key ingredient?
- The primary active component is Poly-L-lactic Acid (PLLA) at 360mg per vial, a biodegradable and biocompatible polymer in spherical particle form that encourages the body to produce its own collagen for natural, gradual improvement.
- How is MENNUS PLUS prepared?
- The 360mg PLA powder is reconstituted with 8-10ml of sterile distilled water and 1-2ml of 2% Lidocaine. The solution is withdrawn with an 18G needle and injected using a 26G needle or 25G cannula into the superficial dermal to subcutaneous layer. Freeze-drying technology enables faster dilution.
- How long do results last?
- The initial volume effect lasts 3-9 months, while collagen regeneration provides lasting results for 18-24 months. A course of 1-3 sessions is recommended depending on individual needs.
- Who should administer MENNUS PLUS?
- MENNUS PLUS is for professional use and should be administered with proper technique and aftercare. It should be avoided in patients with a history of keloid formation or hypertrophic scarring, and common injection-related reactions may include swelling, pain, or hemorrhage.
METOX 100 Units (1 Vial)
3700
$37.00
Unit price perMETOX 100 Units (1 Vial)
3700
$37.00
Unit price per
METOX
1 Vial - 100 Units
Clostridium Botulinum Toxin Type A
Clostridium Botulinum Toxin Type A
Premium Cosmetic & Therapeutic Botulinum Toxin
Highly purified botulinum toxin designed for both cosmetic and therapeutic applications. Advanced vacuum dehydration technology ensures superior stability and proven efficacy for professional medical use.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Product packaging and vial image placeholder
High Purity
Advanced Botulinum Toxin Formula
METOX 100U is manufactured with vacuum dehydration technology to ensure high purity and stability. This advanced process minimizes denaturation during dilution and provides reliable, consistent results for long-term treatments.
- Improvement of frown lines, crow's feet, and forehead wrinkles
- Treatment for hyperhidrosis (excessive sweating)
- Enhancement of lip contouring and neck wrinkle reduction
- Professional-grade formula with minimized resistance risk
Ingredients & Composition
- Clostridium Botulinum Toxin Type A
- 100 Units Primary active ingredient for muscle relaxation and wrinkle reduction
- Human Serum Albumin
- Stabilizer Protein stabilizer to maintain toxin integrity during storage
- Sodium Chloride
- Excipient Maintains osmotic balance and ensures safe injection
Mechanism of action infographic placeholder
Vacuum Dehydration Technology
Advanced manufacturing process ensures high potency and stability, reducing the risk of protein denaturation and maintaining consistent therapeutic efficacy across treatments.
Treatment Effects & Benefits
3-7 Days
Onset of Effect
1-2 Weeks
Maximum Effect
6-9 Months
Duration
- Relaxation of moderate to severe facial lines caused by muscle contractions
- Significant improvement in glabellar wrinkles with quick, noticeable results
- Extended duration of aesthetic effects for patient satisfaction
- Proven efficacy in clinical studies with outstanding cosmetic outcomes
Before/After comparison photos placeholder
Long-term Treatment Value
High purity formulation minimizes the risk of developing resistance, making METOX 100U suitable for repeated treatments with consistent results over time.
Usage Protocol & Administration
1
Preparation & Reconstitution
Reconstitute vacuum-dried powder with sterile, preservative-free 0.9% normal saline using 2.5ml for 100-unit vial to achieve 4 units/0.1ml concentration.
2
Gentle Mixing
Gently swirl the vial to mix the solution. Do not shake vigorously to prevent protein denaturation.
3
Treatment Area Assessment
Qualified medical professional evaluates treatment area and determines appropriate dosage and injection points.
4
Precise Administration
Administer according to recommended units per treatment area: Glabellar lines (20-30 units), Forehead lines (10-20 units), Crow's feet (10-15 units per side).
5
Post-Treatment Care
Monitor patient response and schedule follow-up. Minimum interval between treatments should be 3 months.
Recommended Dosage Guidelines
Dosage and injection points must be determined by certified medical professionals based on individual patient assessment and treatment objectives.
Treatment areas and injection points guide placeholder
Storage & Handling Specifications
| Storage Condition | Temperature | Duration |
|---|---|---|
| Unopened Vial | 2-8°C (Refrigerated) | Until Expiration Date |
| Reconstituted Solution | 2-8°C (Refrigerated) | Within 24 Hours |
| Room Temperature | Not Recommended | Avoid |
Professional Use Requirements
This product must be administered by certified and trained medical professionals only. Do not mix with other solutions unless directed by professional guidelines.
100 Units
Per Vial
24 Hours
Use After Reconstitution
2-8°C
Storage Temperature
Safety Precautions & Warnings
Important Safety Information
Professional medical supervision required. Not suitable for all patients.
- Do not use on pregnant or breastfeeding individuals
- Avoid use in patients with known hypersensitivity to ingredients
- Minimum 3-month interval between treatments required
- Discard any unused portion after 24 hours of reconstitution
Contraindications
Not recommended for patients with neuromuscular disorders, active skin infections at injection sites, or known allergies to botulinum toxin products.
Professional Administration Only
Must be administered by qualified healthcare professionals with proper training in botulinum toxin injection techniques and facial anatomy knowledge.
Frequently Asked Questions
- What is METOX 100U used for?
- METOX 100U is used to improve frown lines, crow's feet, and forehead wrinkles. It is also applied for hyperhidrosis (excessive sweating), lip contouring, and neck wrinkle reduction.
- How soon does METOX 100U work and how long do results last?
- Onset of effect is typically seen within 3-7 days, with maximum effect at 1-2 weeks. Results generally last 6-9 months, varying by patient and treatment area.
- What is the standard dilution for METOX 100U?
- Reconstitute with 2.5 mL of sterile, preservative-free 0.9% normal saline to achieve a concentration of 4 units per 0.1 mL.
- Who should administer METOX 100U?
- METOX must be administered by certified medical professionals trained in injection technique and facial anatomy. It is contraindicated in pregnancy or breastfeeding, neuromuscular disorders, active skin infection at the injection site, and known hypersensitivity to botulinum toxin.
METOX 200 Units (1 Vial)
5800
$58.00
Unit price perMETOX 200 Units (1 Vial)
5800
$58.00
Unit price per
METOX
1 Vial - 200 Units
Clostridium Botulinum Toxin Type A
Clostridium Botulinum Toxin Type A
Premium Cosmetic & Therapeutic Botulinum Toxin
METOX 200 Units is a revolutionary product formulated with Botulinum Toxin Type A, meticulously crafted to address dynamic wrinkles and fine lines effectively. Engineered to deliver unparalleled results, METOX 200 Units offers a rejuvenating experience that restores youthful vibrance to your skin.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Product packaging and vial image placeholder
High Purity
Advanced Botulinum Toxin Formula
METOX 200U is manufactured with vacuum dehydration technology to ensure high purity and stability. This advanced process minimizes denaturation during dilution and provides reliable, consistent results for long-term treatments.
- Improvement of frown lines, crow's feet, and forehead wrinkles
- Treatment for hyperhidrosis (excessive sweating)
- Enhancement of lip contouring and neck wrinkle reduction
- Professional-grade formula with minimized resistance risk
Ingredients & Composition
- Clostridium Botulinum Toxin Type A
- 200 Units Primary active ingredient for muscle relaxation and wrinkle reduction
- Human Serum Albumin
- Stabilizer Protein stabilizer to maintain toxin integrity during storage
- Sodium Chloride
- Excipient Maintains osmotic balance and ensures safe injection
Mechanism of action infographic placeholder
Vacuum Dehydration Technology
Advanced manufacturing process ensures high potency and stability, reducing the risk of protein denaturation and maintaining consistent therapeutic efficacy across treatments.
Treatment Effects & Benefits
3-7 Days
Onset of Effect
1-2 Weeks
Maximum Effect
6-9 Months
Duration
- Temporarily relaxes specific facial muscles to smooth dynamic wrinkles and improve facial symmetry
- Precision Delivery : Engineered for accurate, targeted administration
- Long-Lasting Effects : Provides smooth, natural-looking results that endure
- Clinically Proven : Backed by scientific research and extensive clinical trials
Before/After comparison photos placeholder
Long-term Treatment Value
High purity formulation minimizes the risk of developing resistance, making METOX 200U suitable for repeated treatments with consistent results over time.
Usage Protocol & Administration
1
Preparation & Reconstitution
Reconstitute vacuum-dried powder with sterile, preservative-free 0.9% normal saline using 5ml for the 200-unit vial to achieve 4 units/0.1ml concentration.
2
Gentle Mixing
Gently swirl the vial to mix the solution. Do not shake vigorously to prevent protein denaturation.
3
Treatment Area Assessment
Qualified medical professional evaluates treatment area and determines appropriate dosage and injection points.
4
Precise Administration
Administer according to recommended units per treatment area: Glabellar lines (20-30 units), Forehead lines (10-20 units), Crow's feet (10-15 units per side).
5
Post-Treatment Care
Monitor patient response and schedule follow-up. Minimum interval between treatments should be 3 months.
Recommended Dosage Guidelines
Dosage and injection points must be determined by certified medical professionals based on individual patient assessment and treatment objectives.
Treatment areas and injection points guide placeholder
Storage & Handling Specifications
| Storage Condition | Temperature | Duration |
|---|---|---|
| Unopened Vial | 2-8°C (Refrigerated) | Until Expiration Date |
| Reconstituted Solution | 2-8°C (Refrigerated) | Within 24 Hours |
| Room Temperature | Not Recommended | Avoid |
Professional Use Requirements
This product must be administered by certified and trained medical professionals only. Do not mix with other solutions unless directed by professional guidelines.
200 Units
Per Vial
24 Hours
Use After Reconstitution
2-8°C
Storage Temperature
Safety Precautions & Warnings
Important Safety Information
Professional medical supervision required. Not suitable for all patients.
- Do not use on pregnant or breastfeeding individuals
- Avoid use in patients with known hypersensitivity to ingredients
- Minimum 3-month interval between treatments required
- Discard any unused portion after 24 hours of reconstitution
Contraindications
Not recommended for patients with neuromuscular disorders, active skin infections at injection sites, or known allergies to botulinum toxin products.
Professional Administration Only
Must be administered by qualified healthcare professionals with proper training in botulinum toxin injection techniques and facial anatomy knowledge.
Frequently Asked Questions
- What is METOX 200U used for?
- METOX 200U is used to improve frown lines, crow's feet, and forehead wrinkles. Its higher unit count also supports hyperhidrosis (excessive sweating), lip contouring, and neck wrinkle reduction, as well as larger treatment areas.
- How soon does METOX 200U work and how long do results last?
- Onset of effect is typically seen within 3-7 days, with maximum effect at 1-2 weeks. Results generally last 6-9 months, varying by patient and treatment area.
- What is the standard dilution for METOX 200U?
- Reconstitute with 5 mL of sterile, preservative-free 0.9% normal saline to achieve a concentration of 4 units per 0.1 mL — the same concentration as a 2.5 mL dilution of a 100-unit vial.
- Who should administer METOX 200U?
- METOX must be administered by certified medical professionals trained in injection technique and facial anatomy. It is contraindicated in pregnancy or breastfeeding, neuromuscular disorders, active skin infection at the injection site, and known hypersensitivity to botulinum toxin.
MOMM mini Body Filler (70cc × 1 Vial)
8100
$81.00
Unit price perMOMM mini Body Filler (70cc × 1 Vial)
8100
$81.00
Unit price per
Product Identification
MOMM mini 70cc
High-Viscosity Body Filler
Daejong Meditec Sterile HA Gel PDMP Technology
Total Volume/Content
70mL × 1 Vial (Bottle)
Packaging Type
Glass Vial (Standard Bottle)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Active Ingredients
Cross-linked Hyaluronic Acid 20mg/mL + Lidocaine 0.3%
Key Technology: PDMP
Precise Duplex Mesh Process (PDMP) ensures high viscosity and cohesiveness for long-lasting volume. Supported by LCCP (Low Concentration Cross-linking Process) to minimize residue.
PDMP Technology High Viscosity Lidocaine Included
Efficacy & Benefits
Main Effects
- Body Contouring: Non-surgical augmentation of breasts and buttocks.
- Volume Restoration: Effectively fills deep depressions, hip dips, and corrects asymmetry.
- Shape Correction: Enhances overall body curves and profile.
Recommended Areas
Buttocks, Hips, Breasts, and other large body areas requiring volume.
Usage Protocol
Application Method
Deep Subcutaneous or Supraperiosteal injection using a Cannula (18G–24G) due to high viscosity.
Duration of Effect
Typically 10–18 months, depending on individual metabolism and lifestyle.
Treatment Cycle
Single session provides immediate volume; touch-ups can be done as needed.
MOMM Series Comparison
| Product | Volume | Packaging | Recommended Use |
|---|---|---|---|
| MOMM mini | 70mL | Glass Vial (Bottle) | Moderate volume, Specific corrections |
| MOMM (Standard) | 100mL | IV-Bag Type | Extensive full-body contouring |
Use MOMM mini (70cc) when a standard vial capacity is sufficient for smaller corrections or specific volume enhancements.
Storage & Handling
Storage Conditions
Room temperature (1–30°C). Store in a cool, shaded place away from direct sunlight. Do not freeze.
Shelf Life
36 months from the manufacturing date.
Safety Information
Contraindications Pregnancy, breastfeeding, hypersensitivity to Hyaluronic Acid or Lidocaine, active skin infection.
Safety Warnings STRICTLY for professional use. Do not inject into blood vessels.
Common Side Effects
- Swelling, bruising, redness, and tenderness at the injection site are common.
Post-Treatment Care
Avoid high heat (sauna) and strenuous exercise for 1–2 weeks. Wear compression garments if advised.
Keywords
MOMM mini MOMM Body Filler 70cc Filler HA Body Filler Buttock Augmentation Breast Filler PDMP Technology Korean Body Filler
Frequently Asked Questions
What is MOMM mini Body Filler used for?
MOMM mini is a high-viscosity body filler used for non-surgical body contouring. It provides augmentation of the breasts and buttocks, fills deep depressions and hip dips, corrects asymmetry, and enhances overall body curves and profile. Recommended areas include the buttocks, hips, and breasts.
What is MOMM mini Body Filler made of?
MOMM mini is made of Cross-linked Hyaluronic Acid 20mg/mL with Lidocaine 0.3%. It uses Precise Duplex Mesh Process (PDMP) technology for high viscosity and cohesiveness, supported by LCCP (Low Concentration Cross-linking Process) to minimize residue.
How long do results from MOMM mini Body Filler last?
A single session provides immediate volume, and results typically last 10–18 months depending on individual metabolism and lifestyle.
Who should administer MOMM mini Body Filler?
MOMM mini is strictly for professional use, administered by deep subcutaneous or supraperiosteal injection using a cannula (18G–24G) due to its high viscosity. It must not be injected into blood vessels. It is contraindicated in pregnancy, breastfeeding, hypersensitivity to Hyaluronic Acid or Lidocaine, and active skin infection.
Who manufactures MOMM mini Body Filler?
MOMM mini is manufactured by Daejong Meditec.