100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
COLLECTION
Anti-aging and Wrinkle Care
Turn back the clock with our anti-aging and wrinkle care collection. Our K-Derma products are expertly formulated to smooth fine lines, firm sagging skin, and restore a more youthful and radiant look.
122 products
122 products
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CHAEUM PREMIUM (No.1 / No.2 / No.3 / No.4)
5300
$53.00
Unit price perCHAEUM PREMIUM (No.1 / No.2 / No.3 / No.4)
5300
$53.00
Unit price per
CHAEUM PREMIUM
No.1 / No.2 / No.3 / No.4
High-quality product photography showing CHAEUM PREMIUM syringe packaging with elegant medical aesthetic
CHAEUM PREMIUM No.1
2 x 1.1 ml syringes
CHAEUM PREMIUM No.2
2 x 1.1 ml syringes
CHAEUM PREMIUM No.3
2 x 1.1 ml syringes
CHAEUM PREMIUM No.4
2 x 1.1 ml syringes
Premium Hyaluronic Acid Dermal Filler
Advanced BDDE cross-linking technology for natural-looking facial enhancement and wrinkle correction
Hyaluronic Acid Hugel Pharma With Lidocaine
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Technology
BDDE cross-linking for superior performance
Monophasic and even HA structure ensures optimal distribution and natural-looking results with enhanced durability
Lidocaine
Enhanced patient comfort during treatment
0.3% Lidocaine concentration provides effective pain management for comfortable procedures
Quality
Manufactured by Hugel Pharma, South Korea
Rigorous quality control and advanced manufacturing standards ensure consistent, reliable results
Key Ingredients & Formulation
Cross-linked Hyaluronic Acid
20 mg/ml
Highly purified hyaluronic acid with advanced BDDE cross-linking technology creates a monophasic gel structure for optimal tissue integration and natural-looking results. The varying cross-linking rates across the product line provide specific performance characteristics for different treatment areas.
Lidocaine Hydrochloride
0.3% (3 mg/ml)
Local anesthetic integrated into the gel formulation to minimize discomfort during injection procedures. Provides immediate pain relief while maintaining the integrity of the hyaluronic acid structure for enhanced patient experience.
Molecular structure diagram showing BDDE cross-linked hyaluronic acid chain formation and gel architecture
Clinical Benefits & Applications
Primary Applications
-
Wrinkle CorrectionEffective treatment for fine to deep wrinkles with long-lasting results
-
Facial VolumizationRestores lost volume and enhances facial contours for youthful appearance
-
Lip EnhancementNatural lip augmentation with precise volume control and definition
-
Facial RejuvenationComprehensive facial revitalization through targeted treatment approach
Technical Advantages
-
Even DistributionRegular and dense gel structure ensures uniform treatment results
-
Natural IntegrationMonophasic formulation blends seamlessly with natural tissue
-
Minimal InflammationHigh purity formulation reduces post-injection inflammatory response
-
Extended DurationAdvanced cross-linking provides lasting results from 6-12+ months
Before and after treatment comparison photos showing natural-looking enhancement results across different facial areas
Product Variants & Treatment Guide
CHAEUM PREMIUM No.1
Viscosity: Low | Injection Layer: Superficial to mid-dermis | Needle: 30G
Treatment Areas: Fine wrinkles such as glabellar lines, periorbital and perioral lines, lip contouring, skin rejuvenation
Duration: 6-8 months | Ideal for smoothing fine wrinkles and improving skin texture with a natural finish
Treatment Areas: Fine wrinkles such as glabellar lines, periorbital and perioral lines, lip contouring, skin rejuvenation
Duration: 6-8 months | Ideal for smoothing fine wrinkles and improving skin texture with a natural finish
CHAEUM PREMIUM No.2
Viscosity: Medium | Injection Layer: Middle and superficial dermis | Needle: 27G
Treatment Areas: Glabellar and forehead lines, periorbital and perioral wrinkles, lip augmentation
Duration: 6-9 months | Ideal for medium wrinkles and lip enhancement with seamless injection in sensitive areas
Treatment Areas: Glabellar and forehead lines, periorbital and perioral wrinkles, lip augmentation
Duration: 6-9 months | Ideal for medium wrinkles and lip enhancement with seamless injection in sensitive areas
CHAEUM PREMIUM No.3
Viscosity: High | Injection Layer: Middle and deep dermis | Needle: 25G
Treatment Areas: Nasolabial folds, chin wrinkles, facial volumization (forehead, chin, cheekbones), nose bridge
Duration: 8-12 months | High cross-linking rate provides strong lifting effect for areas requiring more support
Treatment Areas: Nasolabial folds, chin wrinkles, facial volumization (forehead, chin, cheekbones), nose bridge
Duration: 8-12 months | High cross-linking rate provides strong lifting effect for areas requiring more support
CHAEUM PREMIUM No.4
Viscosity: Very High | Injection Layer: Deep subcutaneous layer | Needle: 23G
Treatment Areas: Facial contouring, volume augmentation (chin, cheeks, cheekbones, temples), chin correction
Duration: 12+ months | Highest cross-linking rate for substantial lift and structural shaping
Treatment Areas: Facial contouring, volume augmentation (chin, cheeks, cheekbones, temples), chin correction
Duration: 12+ months | Highest cross-linking rate for substantial lift and structural shaping
| Product Version | Viscosity | Injection Layer | Needle Gauge | Duration |
|---|---|---|---|---|
| CHAEUM PREMIUM No.1 | Low | Superficial Dermis | 30G | 6-8 months |
| CHAEUM PREMIUM No.2 | Medium | Middle & Superficial Dermis | 27G | 6-9 months |
| CHAEUM PREMIUM No.3 | High | Middle & Deep Dermis | 25G | 8-12 months |
| CHAEUM PREMIUM No.4 | Very High | Deep Subcutaneous | 23G | 12+ months |
Facial mapping diagram showing optimal injection sites and treatment areas for each product variant
Professional Treatment Guidelines
Pre-Treatment Preparation
Assess treatment area and select appropriate product variant based on desired outcome. Ensure sterile conditions and prepare injection equipment. Verify patient medical history and obtain informed consent for procedure.
Injection Technique
Use recommended needle gauge for selected product variant. Inject slowly into appropriate tissue layer with proper angle and depth. Monitor gel distribution and adjust technique as needed for optimal results.
Post-Treatment Care
Apply gentle pressure if needed to achieve desired contour. Provide post-treatment instructions including activity restrictions and follow-up schedule. Monitor for any adverse reactions or complications.
Step-by-step injection technique demonstration showing proper needle placement and gel distribution methods
Safety Information & Precautions
Important Safety Guidelines
For professional use only. This product should only be administered by qualified healthcare professionals with appropriate training in dermal filler injection techniques. Store at room temperature and use immediately upon opening. Single-use product - do not reuse or resterilize.
Post-Treatment Precautions
Patients should avoid touching or massaging the treated area for 24 hours. Refrain from strenuous physical activity, alcohol consumption, and exposure to extreme heat or cold for 48 hours. Mild redness, swelling, or bruising at injection site is normal and typically resolves within a few days.
Contraindications
Do not use if pregnant or breastfeeding. Not recommended for patients with known hypersensitivity to hyaluronic acid or lidocaine. Avoid in areas with active skin infection or inflammation. Consult medical professional for complete list of contraindications and drug interactions.
Safety symbols and proper storage guidelines with temperature and handling requirements
Storage & Handling Instructions
Storage Conditions
Store at room temperature in original packaging. Protect from direct sunlight and extreme temperatures. Do not freeze or expose to temperatures above 25°C (77°F). Keep in dry environment away from moisture.
Handling Guidelines
Handle syringes with care to prevent damage. Use sterile technique when preparing for injection. Check product integrity before use - do not use if packaging is damaged or product appears compromised.
Shelf Life Information
Product maintains stability and effectiveness when stored under recommended conditions. Check expiration date before use. Single-use product - discard after opening and do not attempt to preserve for future use.
Manufacturer & Quality Assurance
Hugel Pharma Co., Ltd. South Korea ISO Certified
Manufactured by Hugel Pharma Co., Ltd., a leading pharmaceutical company in South Korea specializing in advanced dermal filler technology and aesthetic medicine solutions.
Quality assurance through rigorous testing protocols and compliance with international pharmaceutical manufacturing standards. Each batch undergoes comprehensive quality control testing to ensure consistent performance and safety.
Hugel Pharma manufacturing facility and quality control laboratory showcasing advanced production capabilities
Frequently Asked Questions
What is CHAEUM PREMIUM used for?
CHAEUM PREMIUM is a hyaluronic acid dermal filler series used for wrinkle correction, facial volumization, lip enhancement and facial rejuvenation. No.1 treats fine wrinkles and skin rejuvenation, No.2 handles medium wrinkles and lip augmentation, No.3 addresses nasolabial folds and facial volumization, and No.4 is for facial contouring and structural volume augmentation.
What is CHAEUM PREMIUM made of?
CHAEUM PREMIUM is made of highly purified cross-linked hyaluronic acid at 20 mg/ml with 0.3% (3 mg/ml) lidocaine hydrochloride. It uses advanced BDDE cross-linking technology to create a monophasic, even gel structure, with varying cross-linking rates across the product line.
How long do results from CHAEUM PREMIUM last?
Results last from 6 to 12+ months depending on the variant: approximately 6-8 months for No.1, 6-9 months for No.2, 8-12 months for No.3, and 12+ months for No.4.
Who should administer CHAEUM PREMIUM?
CHAEUM PREMIUM is for professional use only and should only be administered by qualified healthcare professionals trained in dermal filler injection techniques. It should not be used during pregnancy or breastfeeding, in patients with known hypersensitivity to hyaluronic acid or lidocaine, or in areas with active skin infection or inflammation.
Who manufactures CHAEUM PREMIUM?
CHAEUM PREMIUM is manufactured by Hugel Pharma Co., Ltd. in South Korea.
OLIDIA (PLLA 365mg × 1 Vial)
12000
$120.00
Unit price perOLIDIA (PLLA 365mg × 1 Vial)
12000
$120.00
Unit price per
Collagen Stimulator
PLLA Filler
PRP Life Science
Advanced Neocollagenesis Technology
Olidia
Poly-L-Lactic Acid (PLLA) 365mg x 1 Vial
Biocompatible collagen stimulator for long-lasting facial volume restoration and wrinkle correction
#Biodegradable
#Long-Lasting
#Natural Results
#Volume Restoration
OLIDIA Product Vial Visual
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Active Ingredients & Composition
OLIDIA contains pure Poly-L-Lactic Acid (PLLA), a biocompatible and biodegradable synthetic polymer that stimulates natural collagen production through controlled neocollagenesis.
Poly-L-Lactic Acid (PLLA)
Primary collagen-stimulating polymer that promotes fibroblast activation
365mg per vial
Sterile Water for Injection
Reconstitution medium for creating injectable suspension
As required
Lidocaine (Optional)
Local anesthetic to minimize injection discomfort
1-2mL recommended
PLLA Molecular Structure & Mechanism Visualization
Mechanism of Action
PLLA particles act as a biodegradable scaffold that stimulates fibroblasts to produce new collagen. The gradual degradation process ensures sustained collagen synthesis over an extended period, providing natural-looking, long-lasting results.
Biocompatibility
FDA-approved synthetic material with excellent tissue tolerance
Degradation Rate
Gradual breakdown over 12-18 months with sustained collagen production
Particle Size
Optimized microsphere dimensions for effective tissue integration
💡 Clinical Benefits & Efficacy
Volume Restoration
Restores lost facial volume through natural collagen regeneration
Wrinkle Correction
Smooths moderate to severe facial wrinkles and folds
Skin Texture Improvement
Enhances overall skin elasticity and texture quality
Long-Lasting Results
Effects maintained for more than 2 years in clinical studies
Nasolabial Folds
Marionette Lines
Cheek Volume
Facial Contouring
Key Treatment Areas
- • Facial wrinkles and folds including nasolabial and marionette lines
- • Cheek volume enhancement for youthful contour restoration
- • Additional applications for neck, hands, and body contouring
- • Overall facial rejuvenation through natural collagen stimulation
OLIDIA Treatment Areas & Results Visualization
Clinical studies demonstrate that 80% of subjects maintained visible improvement for approximately 24 months, with gradual, natural-looking results appearing over several weeks as new collagen forms.
🧪 Application Protocol & Usage Guide
1
Reconstitution
Mix PLLA powder with sterile water for injection and optional lidocaine according to manufacturer guidelines
Mix PLLA powder with sterile water for injection and optional lidocaine according to manufacturer guidelines
2
Preparation
Allow suspension to reach room temperature and ensure complete mixing before injection
Allow suspension to reach room temperature and ensure complete mixing before injection
3
Injection Technique
Inject into deep dermis or subcutaneous tissue using linear threading technique
Inject into deep dermis or subcutaneous tissue using linear threading technique
4
Distribution
Ensure even distribution throughout treatment area for optimal results
Ensure even distribution throughout treatment area for optimal results
5
Post-Treatment Massage
Apply gentle massage for 5 minutes, 5 times daily, for 5 days following treatment
Apply gentle massage for 5 minutes, 5 times daily, for 5 days following treatment
Recommended treatment cycle: 3 sessions at 1-month intervals for optimal collagen stimulation and long-lasting results.
Standard Injection Protocol
- Use 23G or 26G needle for precise injection control
- Target deep dermis to subcutaneous tissue layer
- Apply linear threading technique for even distribution
- Results appear gradually over 4-6 weeks as collagen forms
Advanced Cannula Technique
- Use 25G to 26G cannula with 21G puncture needle guide
- Access deeper tissue planes for enhanced volume restoration
- Multiple entry points for comprehensive area coverage
- Extended results timeline with professional technique mastery
Injection Technique Visual Guide & Depth Illustration
📊 Product Specifications & Storage
365mg
PLLA Content
1 Vial
Package Unit
72 hrs
Use After Reconstitution
Storage Temperature
Room temperature below 30°C (86°F)
Formulation Type
Lyophilized powder for reconstitution
Manufacturer
PRP Life Science Co., Ltd.
Shelf Life
See package labeling for expiration date
🧬 Clinical Evidence & Duration
Clinical Study Results & Duration Timeline Chart
Efficacy Indicators
80%
Subjects Maintained Results at 24 Months
2+
Years Results Duration
100%
Biodegradable & Safe
Clinical studies demonstrate sustained improvement through gradual collagen synthesis. OLIDIA's biocompatible PLLA formulation eliminates the need for pre-treatment allergy testing, making it suitable for most patients.
Results Timeline
Gradual improvement over 4-6 weeks with peak effects at 3-6 months
Duration
Effects maintained for more than 24 months in 80% of subjects
Safety Profile
Synthetic material with no animal-derived components
⚠️ Important Safety Information
OLIDIA should only be administered by qualified healthcare professionals trained in injection techniques. Proper patient assessment and injection protocols are essential for safe and effective treatment.
- Avoid injection into blood vessels to prevent serious complications
- Not recommended for injection into thin skin areas (glabella, periorbital)
- Do not inject into the vermilion border of lips
- Use immediately after reconstitution or within 72 hours if refrigerated
Contraindications & Restrictions
- Avoid areas with active skin infections or inflammation
- Not suitable for patients with autoimmune conditions affecting connective tissue
- Pregnancy and breastfeeding contraindicated
- Areas with high vascularity require special consideration
Post-Treatment Care Instructions
- Perform gentle massage 5 minutes, 5 times daily for 5 days
- Avoid alcohol consumption and smoking during healing period
- Protect treated areas from excessive sun exposure
- Contact healthcare provider if unusual swelling or reactions occur
Post-Treatment Care & Massage Technique Guide
❓ Frequently Asked Questions
A. Unlike traditional fillers that provide immediate volume, OLIDIA stimulates your body's natural collagen production for gradual, long-lasting results that can extend beyond 2 years. The results appear more natural as they develop over weeks. A. Results appear gradually over 4-6 weeks as new collagen forms. Peak effects are typically visible at 3-6 months post-treatment, with continued improvement possible for several months thereafter. A. A typical treatment cycle consists of 3 sessions spaced 1 month apart. This protocol optimizes collagen stimulation and ensures comprehensive volume restoration for long-lasting results. A. OLIDIA's synthetic PLLA formulation is biocompatible and suitable for most skin types. Since it contains no animal-derived ingredients, pre-treatment allergy testing is not required. A. OLIDIA is effective for facial wrinkles, nasolabial folds, marionette lines, and cheek volume restoration. It can also be used for neck, hand, and body contouring applications. A. Common side effects include temporary swelling, bruising, or tenderness at injection sites. These typically resolve within a few days. Following post-treatment massage protocols helps optimize results.
Q. How does OLIDIA differ from traditional dermal fillers?
Q. When will I see results after OLIDIA treatment?
Q. How many treatment sessions are required?
Q. Is OLIDIA suitable for all skin types?
Q. What areas can be treated with OLIDIA?
Q. Are there any side effects or downtime?
🔬 Technical Specifications & Professional Information
| Parameter | Specification | Clinical Significance |
|---|---|---|
| PLLA Content | 365mg per vial | Optimal dosage for effective collagen stimulation |
| Particle Size | Microsphere format | Enhanced tissue integration and biocompatibility |
| Injection Depth | Deep dermis to subcutaneous | Targets optimal tissue layer for volume restoration |
| Needle Gauge | 23G-26G needle / 25G-26G cannula | Precise delivery with minimal trauma |
| Degradation | 12-18 months | Sustained collagen production timeline |
Professional Guidelines
Reconstitution
Sterile water for injection + optional 1-2mL lidocaine
Working Time
Use immediately or within 72 hours if refrigerated
Technique
Linear threading method recommended for optimal distribution
Cross-Linking
No traditional cross-linking - pure PLLA collagen stimulation
Professional Injection Technique & Depth Guide
📈 OLIDIA Advantages & Unique Features
Synthetic Biocompatible Material
No animal-derived components, eliminating allergy testing requirements
Safety First
Long-Lasting Results
Effects maintained for 2+ years through sustained collagen production
24+ Months
Natural Collagen Stimulation
Gradual improvement through body's own collagen synthesis
Neocollagenesis
Versatile Application
Suitable for facial, neck, hand, and body treatments
Multi-AreaKey Differentiators
- • Pure PLLA formulation without traditional cross-linking agents
- • Graduated results that improve over time rather than immediate volume
- • Biodegradable polymer with excellent safety profile
- • Professional-grade concentration optimized for effective collagen stimulation
- • Suitable for comprehensive facial rejuvenation protocols
OLIDIA Results Timeline & Collagen Formation Process
Frequently Asked Questions
Used for
OLIDIA is a PLLA collagen stimulator used for long-lasting facial volume restoration and wrinkle correction, smoothing moderate to severe wrinkles and folds, improving skin texture and elasticity, and rejuvenating areas such as nasolabial folds, marionette lines, and cheeks, as well as neck, hands, and body.
Key ingredient
The active ingredient is pure Poly-L-Lactic Acid (PLLA) at 365mg per vial, a biocompatible and biodegradable synthetic polymer in microsphere form that stimulates fibroblasts to produce new collagen.
How prepared
The lyophilized powder is reconstituted with sterile water for injection plus optional 1-2mL lidocaine, then injected into the deep dermis or subcutaneous tissue using a 23G-26G needle or 25G-26G cannula with linear threading. It is used immediately or within 72 hours if refrigerated.
How long results last
Results appear gradually over 4-6 weeks with peak effects at 3-6 months and are maintained for more than 24 months in 80% of subjects. A cycle of 3 sessions at 1-month intervals is recommended.
Who should administer
OLIDIA should only be administered by qualified healthcare professionals trained in injection techniques. It is contraindicated in pregnancy and breastfeeding, in patients with autoimmune conditions affecting connective tissue, and in areas with active skin infection or inflammation.
Manufacturer
OLIDIA is manufactured by PRP Life Science Co., Ltd.
REGENOVUE PLUS (FINE / DEEP / SUB-Q) (1.1mL × 1 Syringe)
4200
$42.00
Unit price perREGENOVUE PLUS (FINE / DEEP / SUB-Q) (1.1mL × 1 Syringe)
4200
$42.00
Unit price per
NeoGenesis Hyaluronic Acid BDDE Cross-linked 24mg/ml
REGENOVUE PLUS
FINE / DEEP / SUB-Q
Advanced dermal fillers with cross-linked hyaluronic acid for comprehensive facial aesthetic treatments and volume enhancement
Cross-linked HA 24mg/ml - Restore volume, correct wrinkles, and enhance facial contours with precision
[Main Product Image - REGENOVUE Series]
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Professional-grade dermal fillers with highly purified, non-animal based hyaluronic acid technology
Package Contents
- 1.1ml x 1 pre-filled syringe
- Cross-linked Hyaluronic Acid 24mg/ml
- Two needles included per box
- Plus versions available with Lidocaine 0.3%
Key Features
BDDE Cross-linked Monophasic Gel 8-18 Months Lidocaine Option
[Product Overview Image - Three Variants with Packaging]
Composition & Technical Specifications
Active IngredientHighly purified, non-animal based Hyaluronic Acid
Concentration
24mg/ml
Cross-linking MethodBDDE cross-linking with 100% fully cross-linked, monophasic structure
Gel StructureHomogenous monophasic gel with smooth and uniform particle size
Plus Version EnhancementContains Lidocaine 0.3% for comfortable injection experience
Storage ConditionsStore at 2-25°C, away from direct sunlight
Product Variants Comparison
| Version Name | Viscosity | Treatment Area | Injection Layer | Needle Gauge |
|---|---|---|---|---|
| FINE | Low | Fine lines, crow's feet, perioral wrinkles, neck lines | Upper dermis | 30G |
| DEEP | Medium | Medium to deep wrinkles, nasolabial folds, lip augmentation | Lower dermis / upper subcutaneous | 27G |
| SUB-Q | High | Severe wrinkles, deep folds, facial contouring | Lower subcutaneous | 27G or 25G |
[Treatment Areas Diagram - Facial Injection Zones]
REGENOVUE FINE
FINE Fine Lines Superficial Wrinkles
Primary Applications
Targets and reduces fine lines and superficial wrinkles with precision. Lowest viscosity formulation ideal for delicate areas requiring natural-looking enhancement.
Crow's feet Perioral lines Forehead lines Neck lines
Treatment Details
Duration
Approximately 8-12 months
Injection Layer
Upper dermis
Recommended Needle
30G
[REGENOVUE FINE Treatment Areas - Before/After]
REGENOVUE DEEP
DEEP Medium Wrinkles Lip Augmentation
Primary Applications
Corrects medium to deep wrinkles and folds with versatile medium viscosity. Suitable for lip augmentation and facial contouring with balanced structure and softness.
Nasolabial folds Marionette lines Chin wrinkles Lip contouring
Treatment Details
Duration
Approximately 12-18 months
Injection Layer
Lower dermis or superficial subcutaneous layer
Recommended Needle
27G
[REGENOVUE DEEP Treatment Results - Lip and Fold Correction]
REGENOVUE SUB-Q
SUB-Q Facial Contouring Volume Enhancement
Primary Applications
Eliminates severe wrinkles and deep folds with the highest viscosity formulation. Highly effective for facial volume enhancement and structural contouring with maximum support.
Forehead augmentation Cheekbones Chin enhancement Nose bridge
Treatment Details
Duration
Approximately 12-18 months
Injection Layer
Lower subcutaneous layer
Recommended Needle
27G or 25G
[REGENOVUE SUB-Q Facial Contouring Results]
Which Product Is Right for Me?
Choose the appropriate version based on treatment area and required soft tissue volume for optimal results
For Fine Lines & Delicate Areas
Choose REGENOVUE FINE for delicate areas with shallow lines, crow's feet, and superficial wrinkles requiring precise treatment
FINE
For Moderate Wrinkles & Lip Volume
Choose REGENOVUE DEEP for moderate wrinkles, lip augmentation, and areas requiring balanced volume enhancement
DEEP
For Severe Folds & Structural Volume
Choose REGENOVUE SUB-Q for severe folds, structural volume enhancement, and facial contouring requiring maximum support
SUB-Q
Expected Efficacy Benefits
Wrinkle Improvement
Correction of fine to severe wrinkles and folds with natural-looking results
Facial Volume Restoration
Restore lost facial volume and enhance facial contouring with precision
Lip Augmentation
Enhancement and definition of lips with natural movement and feel
Skin Hydration & Texture
Improved skin hydration and texture enhancement for overall skin quality
[Treatment Results Comparison - Before/After Gallery]
Treatment Protocol & Guidelines
Professional Administration
Must be administered by qualified medical professionals with proper injection techniques
Treatment Cycle
Duration Varies
8-18 months depending on product version and individual factors
Injection Method
Direct syringe injection with appropriate needle gauge
Safety Information & Storage
Important Precautions — Must be administered by qualified medical professionals. Patients should disclose any allergies, especially to hyaluronic acid or lidocaine.
Storage Requirements
- Store at 2-25°C away from direct sunlight
- Single-use product - discard any remaining after opening
- Do not freeze or expose to extreme temperatures
- Check expiration date before use
Contraindications
- Known hypersensitivity to hyaluronic acid
- Pregnancy or breastfeeding
- Active skin infections at treatment site
- History of severe allergic reactions
[Storage and Handling Instructions Infographic]
Frequently Asked Questions
- What is REGENOVUE PLUS used for?
- REGENOVUE PLUS is a hyaluronic acid dermal filler used for correcting fine to severe wrinkles and folds, restoring facial volume, facial contouring, and lip augmentation across areas such as crow's feet, perioral lines, neck lines, nasolabial folds, cheekbones, chin, and nose bridge depending on the version.
- What is REGENOVUE PLUS made of?
- REGENOVUE PLUS is made of highly purified, non-animal based, BDDE cross-linked hyaluronic acid at 24mg/ml in a 100% fully cross-linked, homogenous monophasic gel. The Plus versions also contain 0.3% lidocaine for a comfortable injection experience.
- Who manufactures REGENOVUE?
- REGENOVUE is manufactured by NeoGenesis Co., Ltd. in South Korea.
- How long do results from REGENOVUE PLUS last?
- Duration varies by version: REGENOVUE FINE lasts approximately 8-12 months, while REGENOVUE DEEP and SUB-Q last approximately 12-18 months, depending on the product version and individual factors.
- Who should administer REGENOVUE PLUS?
- REGENOVUE PLUS must be administered by qualified medical professionals. It is contraindicated in patients with known hypersensitivity to hyaluronic acid, during pregnancy or breastfeeding, with active skin infections at the treatment site, or with a history of severe allergic reactions.
EYEBELLA (2mL × 1 Syringe)
3400
$34.00
Unit price perEYEBELLA (2mL × 1 Syringe)
3400
$34.00
Unit price per
Product Image
EYEBELLA
2mL x 1 Syringe
Advanced Polynucleotide Eye Rejuvenation
Professional-grade polynucleotide skin booster specifically designed for delicate eye area rejuvenation. Features 1% salmon DNA-derived PN for enhanced collagen production and skin regeneration.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
[Product Image - EYEBELLA 2mL Syringe]
Premium Quality
Advanced Polynucleotide Technology
EYEBELLA is an innovative skin booster containing 1% Polynucleotide (PN) derived from salmon DNA. This advanced formulation is specifically designed for the delicate periorbital area, delivering targeted rejuvenation to address dark circles, fine lines, and skin elasticity concerns.
- Reduces fine lines and wrinkles around the eyes
- Diminishes dark circles and signs of fatigue
- Enhances skin elasticity and firmness
- Promotes natural skin regeneration and barrier strengthening
Key Ingredients & Composition
- Polynucleotide (PN)
- 1% (20mg/2mL) Highly biocompatible regenerative substance purified from salmon DNA. Known for stimulating the skin's self-regeneration process and repairing damaged dermal tissue through enhanced collagen and elastin production.
[Ingredient Visualization - Polynucleotide Structure]
Advanced Regenerative Mechanism
The polynucleotide works at the cellular level to stimulate fibroblast activity, promoting natural collagen synthesis and improving skin texture. This results in restored volume, reduced appearance of fine wrinkles, and enhanced overall skin quality.
Treatment Benefits & Effects
6-12
Months Duration
2-3
Sessions Required
3-4
Weeks Interval
1%
PN Concentration
- Visible improvement in tear trough area appearance
- Enhanced skin firmness and elasticity restoration
- Natural-looking rejuvenation without invasive surgery
- Long-lasting results with minimal downtime
[Before/After Results - Eye Area Improvement]
Long-term Skin Health Benefits
Beyond immediate aesthetic improvements, EYEBELLA works to rebuild the skin's natural barrier function and enhance its biological condition from within, promoting sustained health and resilience of the delicate eye area.
Treatment Protocol & Application
1
Initial Consultation & Assessment
Professional evaluation of skin condition and treatment area to determine optimal injection pattern and dosage.
2
Preparation & Sterilization
Thorough cleansing of treatment area and preparation of sterile injection equipment with appropriate needle gauge selection.
3
Mesotherapy Injection Technique
Precise administration using 30G needles for dark circles or 33G for facial rejuvenation, following professional injection protocols.
4
Post-Treatment Care
Application of appropriate aftercare products and providing patient instructions for optimal healing and results.
5
Follow-up Schedule
Scheduling subsequent sessions at 3-4 week intervals to achieve optimal cumulative results.
Periorbital Area Treatment
Specialized technique for tear trough region focusing on dark circle reduction and volume restoration using precise injection points for optimal distribution.
Full Facial Rejuvenation
Comprehensive facial treatment protocol for overall skin tone and texture improvement, utilizing broader injection patterns for enhanced skin quality.
[Treatment Guide - Injection Zones & Techniques]
Product Specifications
| Specification | Details | Information |
|---|---|---|
| Volume | 2mL per syringe | Single use pre-filled syringe |
| Packaging | 1 syringe per box | Sterile, ready-to-use format |
| Active Ingredient | Polynucleotide 1% | 20mg/2mL concentration |
| Origin | Salmon DNA derived | Highly purified and biocompatible |
| Application | Professional use only | Medical/dermatological clinics |
Storage & Handling Requirements
Store at temperature between 2°C to 25°C, away from direct sunlight. Maintain in cool, dark place with stable temperature. Shelf life approximately 24 months from manufacture date. Do not use if packaging or seal is compromised.
2-25°C
Storage Temperature
24
Months Shelf Life
30G/33G
Recommended Needles
Professional Use & Safety
Professional Use Only
This product is intended for use by qualified medical professionals or dermatologists only. Proper training in injection techniques and safety protocols is required.
- Use sterile injection techniques at all times
- Verify patient medical history and contraindications
- Follow proper dosage and injection protocols
- Maintain cold chain storage requirements
Treatment Contraindications
Not suitable for patients with active skin infections, known allergies to salmon-derived products, pregnancy, breastfeeding, or autoimmune conditions. Professional assessment required before treatment.
Quality Assurance
Manufactured under strict quality control standards. Each batch undergoes rigorous testing for purity, potency, and safety. Traceable lot numbers ensure product authenticity and quality tracking.
Frequently Asked Questions
The revitalizing effects typically last 6-12 months, depending on individual skin condition, age, and lifestyle factors. Regular maintenance treatments help sustain optimal results.
The typical protocol consists of 2-3 sessions with 3-4 week intervals between treatments. This allows for optimal tissue response and cumulative regenerative benefits.
EYEBELLA is designed for minimal downtime. Some patients may experience mild swelling or redness at injection sites, which typically resolves within 24-48 hours.
Unlike traditional fillers that add volume, polynucleotides work by stimulating the skin's natural regeneration processes, promoting collagen production and improving skin quality from within for more natural-looking results.
Ideal candidates are those with fine lines, dark circles, or loss of elasticity around the eyes who seek natural rejuvenation. A professional consultation is required to assess suitability and exclude contraindications.
Technical Documentation
2mL
Syringe Volume
20mg
PN Content
1%
Concentration
Salmon
DNA Source
Manufacturing Standards
Produced in Korea under strict pharmaceutical manufacturing standards. Each batch undergoes comprehensive quality testing including sterility, endotoxin, and potency assessments to ensure consistent product quality and safety.
[Package Specifications & Labeling]
Professional Application Guide
Comprehensive injection techniques, dosage recommendations, and treatment protocols are available in the professional manual. Proper training in mesotherapy techniques is essential for optimal results and patient safety.
REGENOVUE Aqua Shine Plus (3mL × 3 Syringes)
5700
$57.00
Unit price perREGENOVUE Aqua Shine Plus (3mL × 3 Syringes)
5700
$57.00
Unit price per
Product Identification
REGENOVUE Aqua Shine Plus
REGENOVUE Series (Gold)
NeoGenesis Co., Ltd. Sterile Viscoelastic Gel
Total Volume/Content
9mL per box (3mL × 3 Pre-filled Syringes)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
Hyaluronic Acid (HA) 15mg/mL (Minimally Cross-linked)
Key Supportive Ingredients
Buffered Saline Phosphate (PBS) pH 7.0
Mechanism of Action
The minimal cross-linking technology creates a structure that remains in the dermis longer than non-cross-linked HA. This provides sustained deep hydration, structural renewal of the skin matrix, and bio-stimulation of endogenous collagen.
Minimally Cross-linked Long-lasting Hydration Structural Renewal Bio-stimulation
Efficacy Summary & Benefits
Main Effects
- Long-lasting Deep Hydration: Improved moisture retention compared to non-cross-linked boosters.
- Skin Lifting & Tightening: Improves skin elasticity and firmness.
- Wrinkle Reduction: Smoothes fine lines, crow's feet, and micro-wrinkles.
- Skin Tone Improvement: Brightens complexion and reduces dullness.
- Pore Refinement: Helps to narrow enlarged pores.
Targeted Areas
Nasolabial Folds Forehead & Chin Periorbital Area Neck Wrinkles Back of Hands
Usage Protocol
Recommended Application
Mesotherapy (Nappage, Papule, or linear retrograde techniques)
Treatment Cycle
3–4 sessions spaced 3–4 weeks apart
Onset and Duration
Visible results in 1–2 weeks; effects last 6–8 months.
Preparation
Supplied as ready-to-use pre-filled syringes. Ensure strict aseptic technique during administration.
Series Comparison
| Version | Composition | Primary Goal | Duration |
|---|---|---|---|
| Aqua Shine Plus (Gold) | Minimally Cross-linked HA | Sustained Hydration & Lifting | 6–8 Months |
| Aqua Shine (Silver) | Non-crosslinked HA | Immediate "Cinderella" Effect | 3–6 Months |
Select Aqua Shine Plus (Gold) for patients requiring longer-lasting results, deeper hydration, and mild volumizing effects. Use Aqua Shine (Silver) for first-time users or immediate radiance before events.
Storage & Handling
Required Storage Temperature
Room temperature (up to 25°C)
Shelf Life
24 months (2 years) from manufacture date
Handling Tips
Store away from direct sunlight and avoid extreme heat. Do not freeze. Single-use only.
Precautions & Safety
Contraindications Do not use if you have known hypersensitivity to Hyaluronic Acid, are pregnant or breastfeeding, have autoimmune disorders, or have active skin diseases (infection, inflammation, herpes) at the injection site.
Professional Use Only This product is intended for professional use by licensed medical practitioners only. Do not inject into blood vessels.
Common Temporary Side Effects
- Erythema (redness) or swelling at injection site
- Pain, itching, or bruising
- Symptoms usually resolve within a few days
Post-Treatment Care
- Avoid makeup for 12–24 hours.
- Avoid saunas, steam rooms, and intense exercise for 1 week.
- Apply sun protection diligently.
Keywords
REGENOVUE Aqua Shine Plus NeoGenesis Skin Booster Cross-linked Hyaluronic Acid Mesotherapy Hydro-lifting Long-lasting Hydration Anti-aging Korean Dermal Filler
Frequently Asked Questions
What is REGENOVUE Aqua Shine Plus used for?
It is used for long-lasting deep hydration, skin lifting and tightening, wrinkle reduction, skin tone improvement, and pore refinement.
What is REGENOVUE Aqua Shine Plus's key ingredient?
Its primary active ingredient is Hyaluronic Acid (HA) 15mg/mL (minimally cross-linked), buffered with Phosphate Buffered Saline (PBS) pH 7.0.
How long do results last?
Visible results appear in 1–2 weeks and effects last 6–8 months. A course of 3–4 sessions spaced 3–4 weeks apart is recommended.
Who should administer REGENOVUE Aqua Shine Plus?
It is intended for professional use by licensed medical practitioners only.
Who manufactures REGENOVUE Aqua Shine Plus?
REGENOVUE Aqua Shine Plus is manufactured by NeoGenesis Co., Ltd.
LAENNEC Inj (2mL × 10 / 50 Amps)
7800
From $78.00
Unit price perLAENNEC Inj (2mL × 10 / 50 Amps)
7800
From $78.00
Unit price per2mL x 10 / 50 Ampoules
Laennec inj.
Human Placenta Hydrolysate Injection
Advanced regenerative therapy with human placenta hydrolysate for liver function support, cellular rejuvenation, and tissue repair. Professional-grade injection solution containing growth factors, peptides, and essential bioactive compounds.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
LAENNEC Product Package Image
Professional Grade
Advanced Regenerative Injection Therapy
LAENNEC inj contains 112mg of water-soluble Human Placenta Hydrolysate per 2mL ampoule, providing a comprehensive complex of amino acids, peptides, growth factors, vitamins, and minerals for therapeutic applications.
- Supports liver function improvement in chronic liver disease
- Promotes overall cellular rejuvenation and regeneration
- Improves skin elasticity and appearance
- Reduces inflammation and promotes wound healing
Active Ingredients & Composition
- Human Placenta Hydrolysate
- 112mg per 2mL Water-soluble extract containing a rich complex of bioactive compounds including growth factors, peptides, amino acids, vitamins, and minerals that work synergistically for cellular regeneration.
- Growth Factors
- Natural Complex Essential proteins that stimulate cellular growth, division, and tissue repair processes at the molecular level.
- Amino Acids & Peptides
- Complete Profile Building blocks for protein synthesis and cellular metabolism, supporting tissue regeneration and repair mechanisms.
- Vitamins & Minerals
- Essential Complex Cofactors and nutrients that support enzymatic processes and overall cellular health and vitality.
Ingredient Composition Infographic
Mechanism of Action
The hydrolysate works at a cellular level to promote tissue regeneration and repair. It contains bioactive compounds that help suppress inflammatory responses, accelerate cellular metabolism, and stimulate the production of essential structural proteins like collagen and cartilage, leading to a revitalizing effect on cells and tissues.
Therapeutic Applications
Liver
Function Support
Skin
Rejuvenation
Wound
Healing
Anti
Inflammatory
| Target Condition | Symptoms/Situation | Treatment Benefits | Mechanism |
|---|---|---|---|
| Chronic Liver Disease | Need for liver function support | Hepatocyte regeneration | Contains compounds that support liver cell function |
| Skin Aging | Fine lines, wrinkles, dullness, loss of elasticity | Skin rejuvenation | Accelerates cellular metabolism and stimulates collagen production |
| Skin Conditions | Atopic dermatitis, inflammation, scarring | Anti-inflammatory effects | Possesses anti-inflammatory and regenerative properties |
| Musculoskeletal Pain | Tendon or ligament injuries | Enhanced healing | Suppresses immune responses and enhances wound healing |
Before and After Treatment Results
Administration Protocol
Standard Adult Dosage
Standard dose: 2mL once daily
Intensive treatment: 2mL administered 2-3 times daily based on specific condition and medical advice
Intensive treatment: 2mL administered 2-3 times daily based on specific condition and medical advice
Skin Rejuvenation Protocol
Initial phase: Injections twice a week for the first 4 weeks
Maintenance phase: Once weekly injections for sustained results
Maintenance phase: Once weekly injections for sustained results
Administration Methods
• Subcutaneous injection (most common)
• Intramuscular injection
• Intravenous infusion (professional settings)
• Intradermal injections (specialized applications)
• Intramuscular injection
• Intravenous infusion (professional settings)
• Intradermal injections (specialized applications)
Recommended Injection Points for Professional Use
Product Specifications
| Specification | Value | Details |
|---|---|---|
| Package Contents | 10 / 50 Ampoules | Each ampoule contains 2mL of solution |
| Active Ingredient | 112mg per 2mL | Human Placenta Hydrolysate |
| Storage Temperature | 1-30°C | Room temperature storage |
| Container Type | Glass Ampoules | Opaque, sealed containers |
| Administration Route | Injectable | SC, IM, IV, or intradermal |
2mL
Per Ampoule
10 / 50
Total Ampoules
112mg
Active Content
Safety Information & Precautions
Important Safety Information
Professional administration recommended. Carefully review patient history and contraindications before use.
- Do not administer to patients with a predisposition to allergies without professional consultation
- Use caution when injecting to avoid nerves and blood vessels
- If a rash or other allergic symptoms occur, discontinue use immediately
- Risk of transmitting infectious agents, although highly minimized by sterilization and screening, cannot be entirely eliminated
Storage Guidelines
Store in an opaque, sealed container at room temperature (1-30°C). Protect from direct sunlight and extreme temperatures. Check expiration date before use.
Professional Use Only
This product is intended for use by qualified healthcare professionals only. Proper training in injection techniques and emergency response procedures is required.
Storage and Safety Precautions Infographic
Quality Assurance & Certifications
JBP
Manufacturer
Japan Bio Products Co., Ltd.
GMP
Good Manufacturing Practice
Pharmaceutical grade production standards
Sterile
Sterilization Process
Advanced sterilization and screening protocols
Tested
Quality Control
Comprehensive safety and efficacy testing
Regulatory Compliance
LAENNEC inj is manufactured under strict pharmaceutical standards and has been approved for improving liver function in chronic hepatic disease. The product undergoes rigorous quality control testing to ensure safety and efficacy.
Source & Processing
The placenta extract is carefully sourced and processed to ensure safety and efficacy. Advanced sterilization and screening protocols minimize the risk of infectious agents while preserving the biological activity of the active compounds.
Professional Guidelines
Healthcare Provider Information
This product is intended for use by qualified healthcare professionals only. Proper assessment of patient suitability, injection technique training, and emergency response preparation are essential before administration.
Patient Selection Criteria
Suitable for: Adults seeking support for liver health, skin revitalization, and individuals with specific inflammatory or degenerative tissue conditions.
Contraindications: Patients with known allergies to placental extracts or immunocompromised individuals should be evaluated carefully.
Contraindications: Patients with known allergies to placental extracts or immunocompromised individuals should be evaluated carefully.
Monitoring & Follow-up
Regular monitoring of treatment response and potential adverse reactions is recommended. Dosage and frequency adjustments should be made based on individual patient response and therapeutic goals.
Professional Administration Guidelines Chart
Expected Treatment Outcomes
1-2
Weeks Initial Response
4-6
Weeks Visible Improvement
8-12
Weeks Optimal Results
- Enhanced cellular metabolism and energy production
- Improved tissue repair and regeneration capacity
- Reduced inflammatory markers and oxidative stress
- Increased collagen synthesis and skin elasticity
- Enhanced liver function and detoxification capacity
- Overall improvement in cellular health and vitality
Long-term Benefits
Regular treatment with LAENNEC inj may contribute to sustained improvements in cellular function, tissue health, and overall well-being. The regenerative properties of the placental extract support the body's natural healing processes and may help maintain optimal physiological function over time.
Treatment Timeline and Expected Results Chart
Technical Documentation
pH 6.8-7.2
Solution pH Range
2.0mL
Volume per Ampoule
Clear
Solution Appearance
Sterile
Manufacturing Standard
Composition Analysis
The hydrolysate contains a comprehensive range of bioactive substances including growth factors, cytokines, amino acids (glycine, alanine, leucine, etc.), vitamins (B-complex, vitamin C), and essential minerals that work synergistically to promote cellular regeneration and tissue repair.
Stability & Shelf Life
When stored properly in sealed ampoules at room temperature (1-30°C), LAENNEC inj maintains its potency and sterility throughout its shelf life. Protect from direct sunlight and avoid freezing.
Product Packaging and Labeling Specifications
Frequently Asked Questions
LAENNEC can be administered via subcutaneous, intramuscular, intravenous, or intradermal injection depending on the therapeutic goal. Subcutaneous injection is most common for general regenerative therapy, while intradermal injections are preferred for skin rejuvenation treatments.
For general therapeutic use, the standard dose is 2mL once daily. For skin rejuvenation, a typical protocol involves twice-weekly injections for 4 weeks, followed by weekly maintenance doses. Treatment frequency may be adjusted based on individual response and medical supervision.
Patients with known allergies to placental extracts should avoid use. Those with compromised immune systems or autoimmune conditions should be evaluated carefully. Always consult with a qualified healthcare provider before starting treatment.
Store in opaque, sealed containers at room temperature between 1-30°C. Protect from direct sunlight and extreme temperatures. Do not freeze. Check expiration dates before use and dispose of any damaged ampoules.
Most patients experience minimal discomfort during injection. Initial improvements may be noticed within 1-2 weeks, with more significant results typically seen after 4-6 weeks of treatment. Some patients may experience mild injection site reactions, which usually resolve quickly.
Additional Support
For detailed technical information, administration guidelines, or specific clinical questions, healthcare providers should consult the complete prescribing information or contact the manufacturer directly.
Related Treatment Options
Combination Therapy Considerations
LAENNEC inj may be used as part of a comprehensive treatment protocol. The regenerative properties may complement other therapeutic approaches aimed at skin health, liver function support, or tissue repair, but specific combinations should always be determined by a qualified healthcare professional.
Complementary Treatments
Consider discussing with your healthcare provider how LAENNEC therapy might integrate with other regenerative treatments, nutritional support, or lifestyle modifications to optimize therapeutic outcomes.
Treatment Optimization
For best results, maintain a healthy lifestyle, adequate hydration, and follow all post-treatment care instructions provided by your healthcare provider. Regular follow-up appointments help ensure optimal treatment outcomes.
CARATFILL AURORA (5.2mL × 10 Vials)
10650
$106.50
Unit price perCARATFILL AURORA (5.2mL × 10 Vials)
10650
$106.50
Unit price perAdvanced Skin Booster
CARATFILL AURORA
Professional Regenerative Solution
Advanced polynucleotide and hyaluronic acid formula for comprehensive skin revitalization and anti-aging
Trust
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
[CARATFILL AURORA Product Photography - 10 Vials Box Set]
Composition
Key Ingredients
Polynucleotide (PN)
High Grade
Derived from salmon DNA for powerful tissue regeneration. Stimulates natural collagen production and accelerates cellular repair processes for enhanced skin healing and revitalization.
Sodium Hyaluronate (HA)
Medical Grade
Premium medical-grade hyaluronic acid providing intense hydration and skin plumping effects. Maintains optimal moisture levels for improved elasticity and radiance.
Extracellular Matrix (ECM) Components
Active
Specialized components that support collagen and elastin production, promoting skin structural integrity and long-term anti-aging benefits.
Copper Tripeptide-1 & Amino Acids
Synergistic
Advanced peptide complex with essential amino acids that enhance skin repair mechanisms and support natural regenerative processes for optimal results.
[Molecular Structure and Ingredient Synergy Visualization]
Advantages
Key Benefits
1
Skin Regeneration & Collagen Production
Actively stimulates the skin's natural regenerative capabilities through polynucleotide technology, promoting collagen synthesis for improved skin thickness and resilience.
2
Deep Hydration & Elasticity Enhancement
Provides intense hydration through medical-grade hyaluronic acid, improving skin elasticity and creating a more youthful, plump appearance.
3
Fine Lines & Wrinkle Reduction
Effectively reduces the appearance of fine lines and wrinkles by repairing damaged tissue and promoting cellular renewal for smoother skin texture.
4
Brightening & Tone Improvement
Brightens and evens out skin tone for a radiant complexion while accelerating skin repair processes for overall revitalization.
[Before & After Treatment Results and Skin Analysis]
Application
Treatment Areas & Methods
Face Treatment
Comprehensive facial revitalization addressing fine lines, wrinkles, and overall skin texture improvement for enhanced radiance and youthful appearance.
Neck & Décolletage
Extended treatment coverage for neck and décolletage areas, providing consistent skin quality improvement and anti-aging benefits across these delicate regions.
Micro-needling Application
Professional application via micro-needling (MTS), nano-needles, or direct injection methods for optimal ingredient penetration and treatment efficacy.
[Treatment Area Guide and Application Methods]
Specifications
Product Details
CARATFILL AURORA Specifications
Volume per Vial
5.2ml
Vials per Box
10 Vials
Total Volume
52ml
Formulation
Liquid Solution
Storage Temp
2-28°C
Shelf Life
2 Years
Protocol
Recommended Treatment Cycle
1
Initial Treatment Phase
3-5 sessions scheduled at 1-2 week intervals for optimal results. This intensive phase establishes the foundation for skin regeneration and visible improvement.
2
Maintenance Phase
Single maintenance session every 4-6 weeks to sustain treatment benefits and continue progressive skin improvement over time.
3
Full-Face Coverage Design
Each 5.2ml vial is specially formulated to provide complete full-face treatment without requiring additional mixing or supplementary solutions.
4
Biocompatibility & Safety
Highly compatible with human DNA structure, ensuring exceptional safety profile with minimal side effects and enhanced healing response.
[Treatment Schedule Timeline and Protocol Visualization]
Important Safety & Storage Information
Professional use only. Store at temperatures between 2°C and 28°C, away from direct sunlight. Two-year shelf life when stored properly. This product is intended for topical and cosmetic use or research purposes only. Consult a medical professional for any procedures. Suitable for all skin types when administered by qualified professionals.
[Professional Certification and Safety Guidelines]
FAQ
Frequently Asked Questions
What is CARATFILL AURORA used for?
It is a professional regenerative skin booster used to stimulate skin regeneration and collagen production, provide deep hydration and improve elasticity, reduce fine lines and wrinkles, and brighten and even skin tone on the face, neck, and décolletage.
What is CARATFILL AURORA's key ingredient?
Its key ingredients are Polynucleotide (PN) derived from salmon DNA and medical-grade Sodium Hyaluronate (HA), supported by Extracellular Matrix (ECM) components, Copper Tripeptide-1, and amino acids.
How is CARATFILL AURORA administered?
It is administered by professionals via micro-needling (MTS), nano-needles, or direct injection. Each 5.2ml vial provides a full-face treatment, with a recommended initial phase of 3-5 sessions at 1-2 week intervals, then a maintenance session every 4-6 weeks.
Who should administer CARATFILL AURORA?
It is for professional use only and should be administered by qualified professionals.
CARATFILL AURORA Excellence
CARATFILL AURORA represents the pinnacle of regenerative skin care technology, combining polynucleotide science with premium hyaluronic acid for comprehensive anti-aging solutions. This professional-grade formulation delivers natural, long-lasting results through advanced cellular regeneration and hydration enhancement.
Rejuvenex Forte (2.5mL × 6 Amps)
6100
$61.00
Unit price perRejuvenex Forte (2.5mL × 6 Amps)
6100
$61.00
Unit price per
Product Identification
Rejuvenex Forte
High Concentration PDRN Solution
PharmaResearch Co., Ltd. Ethical Drug (ETC)
Total Volume/Content
2.5mL × 6 Ampoules per Box
Formulation Type
Sterile, transparent, colorless liquid solution in glass ampoules
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredient
Polydeoxyribonucleotide Sodium (PDRN) 14.06mg per 2.5mL
Source Material
DNA derived from the sperm of Salmon (Oncorhynchus keta or Oncorhynchus masou)
Mechanism of Action
- A2A Receptor Activation: PDRN binds to adenosine A2A receptors to exert anti-inflammatory effects and repair damaged tissues.
- Salvage Pathway: Provides nucleosides (DNA precursors) via the salvage pathway to promote rapid DNA synthesis and cell proliferation.
- Growth Factor Stimulation: Promotes the secretion of VEGF and other growth factors to aid angiogenesis and wound healing.
High Concentration (5.6mg/mL) Rapid Regeneration Anti-inflammatory
Efficacy & Benefits
Main Effects (Medical & Aesthetic)
- Tissue Regeneration: Repairs damaged skin barrier, improves skin thickness, and treats ligament/tendon injuries.
- Pore & Scar Reduction: Diminishes acne scars and tightens pores.
- Rapid Healing: Accelerates wound healing and provides anti-inflammatory support.
- Texture Improvement: Enhances overall skin texture and hydration.
Targeted Areas
Face (Acne scars, damaged skin barrier), Body (Stretch marks, surgical wounds).
Usage Protocol
Recommended Application Methods
- Medical (Systemic/Local): Intramuscular (IM) or Subcutaneous (SC) injection.
- Aesthetic (Off-label): Intradermal (ID) injection (Mesotherapy) or MTS (Microneedling) application to the face.
Treatment Cycle
Typically 1 session per week for 3–5 weeks. Tissue regeneration effects are cumulative.
Onset of Effect
Visible skin improvements are often noted after 3–4 sessions.
Preparation Instructions Carefully snap the neck of the glass ampoule using a breaker or gauze to avoid injury. Use a filter needle to draw up the solution to prevent glass particulate contamination.
Series Comparison
| Product | Volume | PDRN Content | Primary Use |
|---|---|---|---|
| Rejuvenex (Standard) | 3mL × 5 Amps | 5.625mg (Low) | General maintenance, Healing |
| Rejuvenex Forte | 2.5mL × 6 Amps | 14.06mg (High) | Intensive repair, Deep scars, Ligaments |
Choose Rejuvenex Forte when faster regeneration or treatment of deeper tissue damage (e.g., deep acne scars, ligament injury) is required.
Storage & Handling
Storage Conditions
Room temperature (1–30°C). Store in a hermetic container, shaded from light. Do not freeze.
Shelf Life
36 months from the manufacturing date.
Usage Note
Ampoules are single-use only; discard any remaining solution immediately after opening.
Safety Information
Contraindications Do not use in patients with hypersensitivity to PDRN or Salmon (fish) derivatives.
Safety Warnings Not intended for intravascular injection. Exercise caution when opening glass ampoules to avoid glass fragments; a filter needle is recommended.
Common Temporary Side Effects
- Mild pain, redness, or swelling at the injection site.
- Bruising from the needle insertion.
Frequently Asked Questions
What is Rejuvenex Forte used for?
Rejuvenex Forte is a high-concentration PDRN solution used for tissue regeneration, pore and scar reduction, rapid wound healing with anti-inflammatory support, and overall skin texture improvement.
What is the key ingredient?
The primary active ingredient is Polydeoxyribonucleotide Sodium (PDRN) at 14.06mg per 2.5mL, derived from salmon DNA.
How long do results last?
Visible skin improvements are often noted after 3–4 sessions, and tissue regeneration effects are cumulative. The typical course is 1 session per week for 3–5 weeks.
Who should administer Rejuvenex Forte?
It is an ethical drug (ETC) administered by injection, including intramuscular or subcutaneous injection and aesthetic intradermal (mesotherapy) or MTS application, and should be administered by a qualified medical professional.
Who manufactures Rejuvenex Forte?
Rejuvenex Forte is manufactured by PharmaResearch Co., Ltd.
Keywords
Rejuvenex Forte PDRN Injection Salmon DNA Tissue Regenerator PharmaResearch Acne Scar Treatment Mesotherapy Wound Healing High Concentration PDRN
REJUBEAU Eye Deal (2.5mL × 1 Syringe)
4500
$45.00
Unit price perREJUBEAU Eye Deal (2.5mL × 1 Syringe)
4500
$45.00
Unit price per
Product Identification
REJUBEAU Eye Deal
Rejubeau PN Skin Booster Series
TRACLE INC. Liquid/Gel (Pre-filled Syringe)
Total Volume/Content
2.5mL x 1 Syringe per box
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technical Details
Primary Active Ingredients
Polynucleotide (PN) 1%, Sodium Hyaluronate (HA) 0.5%
Key Secondary/Supportive Ingredients
Glutathione, Collagen Peptides, Mannitol
Mechanism of Action
Polynucleotide (derived from salmon DNA) regenerates tissue and improves skin density in the dermis, while Hyaluronic Acid provides deep hydration. Glutathione acts as an antioxidant to brighten the skin, and Collagen Peptides stimulate elasticity.
Optimized PN & HA Combination Specialized Eye Area Formulation Tissue Regeneration
Efficacy Summary & Expected Benefits
Main Effects and Benefits
Targeted eye rejuvenation including dark circle reduction and brightening. It provides fine wrinkle correction (Crow's feet), strengthens the skin barrier, and offers deep hydration with improved elasticity.
Recommended/Targeted Areas of Use
Under-eye area (Tear troughs), Crow's feet, Neckline, Back of hands, and thin wrinkles on the face.
Usage Protocol & Application Guide
Recommended Application Method
Injection (Mesotherapy / Intradermal injection) using 32G or 33G (4mm length) needle.
Treatment Cycle/Frequency
3 sessions recommended at 20–30 day intervals.
Preparation Instructions
Ready-to-use pre-filled syringe (No reconstitution required).
Specific Treatment Strategy
| Injection Parameter | Recommended Volume |
|---|---|
| Per Under-Eye Zone | 0.5ml ~ 1.0ml |
| Per Injection Point | 0.05ml ~ 0.1ml |
Part of the Rejubeau PN Skin Booster Series (Lineup includes: Eye Deal, PN Healer, Aqua Bomb). This specific protocol is optimized for the Eye Deal variant.
Storage & Handling Instructions
General Handling Tips
Store away from direct sunlight. The product is for single-use only.
Precautions & Safety Notes
Contraindications Do not use if you have a known allergy to salmon or fish products (PN source), are pregnant or breastfeeding, or have active skin infections/inflammation in the treatment area.
Safety Warnings For professional use only. Avoid injecting into blood vessels.
Common Temporary Side Effects
- Temporary redness at the injection site
- Swelling or bruising
- Tenderness
Post-Treatment Care
- Avoid heavy makeup for a few hours post-injection
- Avoid touching the treated area
Keywords & Search Terms
Rejubeau Eye Deal PN Skin Booster Polynucleotide Injection Under Eye Filler Dark Circle Treatment Salmon DNA Injection TRACLE INC Korean Skin Booster
Frequently Asked Questions
What is REJUBEAU Eye Deal used for?
It is used for targeted eye rejuvenation, including dark circle reduction, brightening, fine wrinkle correction (Crow's feet), skin barrier strengthening, and deep hydration with improved elasticity.
What is REJUBEAU Eye Deal's key ingredient?
Its primary active ingredients are Polynucleotide (PN) 1% (derived from salmon DNA) and Sodium Hyaluronate (HA) 0.5%.
How is REJUBEAU Eye Deal administered?
It is administered by injection (mesotherapy / intradermal injection) using a 32G or 33G (4mm length) needle, with 3 sessions recommended at 20–30 day intervals.
Who should administer REJUBEAU Eye Deal?
It is for professional use only and should be administered by a qualified practitioner.
Who manufactures REJUBEAU Eye Deal?
REJUBEAU Eye Deal is manufactured by TRACLE INC.
LAPUROON AURORA Vivid (5mL × 5 Vials)
8200
$82.00
Unit price perLAPUROON AURORA Vivid (5mL × 5 Vials)
8200
$82.00
Unit price perProfessional Skin Booster
LAPUROON AURORA Vivid
5mL x 5 Vials
Advanced skin regeneration booster with PDRN and Hyaluronic Acid for deep dermal restoration and natural radiance enhancement
PDRN 0.2%
HYALURONIC ACID 1%
PROFESSIONAL USE
This all-in-one skin booster is formulated to awaken your skin's natural glow from within
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Active Ingredients
- Primary Active Complex
- PDRN (Polydeoxyribonucleotide) and Hyaluronic Acid work synergistically to promote fundamental skin regeneration and deep hydration.
- Enhancement & Support System
- Antioxidant-rich blend designed to boost collagen production and provide comprehensive skin barrier protection.
PDRN 0.2%
Hyaluronic Acid 1%
Multi-Peptide Complex
Retinol
Glutathione
Ascorbic Acid (Vitamin C)
Amino Acids
Vitamins & Minerals
-
Deep Dermal Penetration
Patented technology enhances penetration of active ingredients into deep skin layers for maximum regenerative effects. -
Cell Regeneration
PDRN stimulates cellular repair and regeneration while hyaluronic acid provides intense moisture retention. -
Antioxidant Protection
Comprehensive vitamin complex strengthens skin barrier and provides protection against environmental damage.
Expected Efficacy
- Promotes fundamental skin regeneration and repair from deep within the dermis
- Provides intense hydration and moisture, improving rough and dry skin texture
- Enhances skin's natural radiance and glow for a brighter complexion
- Stimulates collagen and elastin synthesis to improve firmness and reduce fine lines
- Strengthens the skin barrier and provides comprehensive antioxidant protection
Anti-Aging
Hydrating
Regenerating
Results show improved skin elasticity, enhanced radiance, and smoother texture with longer-lasting glow and revitalized appearance.
Treatment Protocol
Treatment Planning
Assess skin condition and determine appropriate treatment areas. Suitable for entire face, neck, décolleté, eye area, and back of hands.
Assess skin condition and determine appropriate treatment areas. Suitable for entire face, neck, décolleté, eye area, and back of hands.
Professional Application
Administer via micro-injections into the dermis using MTS or nano-needle techniques for optimal penetration.
Administer via micro-injections into the dermis using MTS or nano-needle techniques for optimal penetration.
Treatment Schedule
Complete series of 3-5 sessions with each session spaced 3-4 weeks apart for maximum effectiveness.
Complete series of 3-5 sessions with each session spaced 3-4 weeks apart for maximum effectiveness.
Post-Treatment Care
Follow aftercare guidelines to ensure optimal results and maintain skin health during recovery period.
Follow aftercare guidelines to ensure optimal results and maintain skin health during recovery period.
Recommended Treatment Cycle
3-5 sessions, 3-4 weeks apart
Treatment Areas
Face, neck, décolleté, eye area, hands
Application Method
Micro-injections, MTS, nano-needles
Professional Use Only
Qualified practitioners required
Product Specifications
| Component | Concentration | Function | Benefits |
|---|---|---|---|
| PDRN | 0.2% | Cell Regeneration | Tissue repair & healing |
| Hyaluronic Acid | 1% | Deep Hydration | Moisture retention |
| Peptides | Multi-complex | Collagen Boost | Firmness & elasticity |
| Retinol | Active dose | Skin Renewal | Texture improvement |
Packaging & Storage Specifications
- Formulation: 5 mL sterile vials, 5 vials per treatment box
- Storage: Cool, dry place away from direct sunlight
- Shelf Life: Follow manufacturer's expiration date
- Professional Use: Licensed practitioners only
Each vial contains precisely measured doses for professional treatment applications with optimal potency preservation.
Safety & Precautions
Professional Use Only — This product is intended for use by qualified medical practitioners. Proper training and certification required.
Contraindications — Do not use if allergic to any ingredients. Not suitable for areas with active infections, acne, or inflammation. Pregnant or breastfeeding individuals should consult medical professional.
Expected Side Effects — Mild redness, swelling, or bruising may occur at injection sites and typically resolves within 2-3 days.
Post-Treatment Care — Avoid direct sun exposure, strenuous activity, saunas, and hot baths for 24-48 hours. Keep treated area clean and moisturized.
Comprehensive safety protocols ensure optimal treatment outcomes and minimize potential adverse reactions.
Frequently Asked Questions
What is LAPUROON AURORA Vivid used for?
It is a professional skin booster for deep dermal regeneration and hydration, enhancing skin's natural radiance, improving firmness and texture, and providing antioxidant protection on the face, neck, décolleté, eye area, and back of hands.
What is LAPUROON AURORA Vivid's key ingredient?
Its key actives are PDRN (Polydeoxyribonucleotide) at 0.2% and Hyaluronic Acid at 1%, supported by a multi-peptide complex, retinol, glutathione, ascorbic acid (Vitamin C), amino acids, and vitamins and minerals.
How is LAPUROON AURORA Vivid administered?
It is administered via micro-injections into the dermis using MTS or nano-needle techniques, over a series of 3-5 sessions spaced 3-4 weeks apart.
Who should administer LAPUROON AURORA Vivid?
It is for professional use only and should be administered by qualified medical practitioners with proper training and certification.
SOONSU Ultra White (3mL x 5 Vials)
8200
$82.00
Unit price perSOONSU Ultra White (3mL x 5 Vials)
8200
$82.00
Unit price per
Product Identification
SOONSU Ultra White
Intensive Skin Whitening & Pigmentation Mesotherapy
Cosmoderma Inc.
Skin Whitening Solution
3mL × 5 Vials
Total Volume/Content
3mL × 5 Vials
Formulation Type
Liquid solution (Mesotherapy / Skin Booster)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
Tranexamoyl Dipeptide-23, Glutathione, Vitamin C, Arbutin, Niacinamide, and Sodium DNA.
Key Secondary/Supportive Ingredients
Peptides (Tetrapeptide, Oligopeptide-2/IGF-1, Polypeptide-1/bFGF), N-Acetyl Glucosamine, and Pantothenic Acid (Vitamin B5).
Mechanism of Action
The active components block the action of tyrosinase (the enzyme responsible for melanin formation) to effectively reduce melanin production. The formula actively integrates with cellular metabolism to deliver progressive multi-step whitening from the surface to the deeper epidermal layer, while peptides and vitamins stimulate skin regeneration and elasticity.
Key Technical Features
Exceptional biocompatibility that is free from cytotoxic effects. It features a stable formulation that minimizes irritation and provides powerful antioxidant defense against environmental damage.
Tyrosinase Inhibitor
Multi-step Whitening
Antioxidant Defense
Efficacy & Benefits
Main Effects
- Intensive skin whitening and brightening.
- Reduction of deep-rooted pigmentation and dark spots.
- Improvement of skin elasticity and texture.
- Pore size reduction and overall anti-aging rejuvenation.
Recommended/Targeted Areas of Use
| Target Area | Primary Indication |
|---|---|
| Face | Melasma, acne scars, and dark circles. |
| Neck | Dull skin and uneven tone. |
| Décolletage | Sun damage and pigmentation. |
| Hands & Elbows | Age spots and severe discoloration. |
Usage Protocol
Recommended Application Method
Professional Mesotherapy injection or MTS (Microneedling Therapy System).
Recommended Dosage per Area
- Face: 1.5–2.0mL
- Neck: 1.0–1.5mL
- Décolletage: 2.0–2.5mL
- Hands: 2.0–3.0mL
Treatment Cycle & Duration
Cycle: Standard mesotherapy protocols generally recommend 3–5 sessions
at 1–2 week intervals.
Duration: Progressively achieves deeper, more pronounced
lightening over time. The anti-aging and brightening benefits are long-lasting, with effects persisting for
up to 9 months.
Preparation Instructions
This product is a ready-to-use solution. No dilution is required.
Storage & Handling
Storage Conditions
Store in a cool and dry place (typically 1–30°C).
General Handling Tips
Keep away from direct sunlight and excessive heat. Intended for professional use; strictly discard any remaining solution after opening a vial.
Safety Information
Contraindications
Pregnancy, breastfeeding, individuals with severe allergies, or active skin infections/inflammation at the
treatment site.
Safety Warnings
Intended for use by certified cosmetologists and medical professionals only to ensure safety. Intravascular
injection is strictly prohibited.
Common Temporary Side Effects
Mild redness, swelling, or pinpoint bruising associated with the injection or microneedling procedure.
Post-Treatment Care
- Apply sunscreen diligently to protect the treated areas and prevent UV-induced pigmentation.
- Avoid direct sunlight, saunas, and harsh environments for a few days post-treatment.
Keywords
SOONSU Ultra White
Skin Whitening
Pigmentation Treatment
Tranexamoyl Dipeptide-23
Glutathione
Arbutin
Vitamin C
Sodium DNA
Cosmoderma
Mesotherapy
Melasma
Frequently Asked Questions
What is SOONSU Ultra White used for?
It is a whitening and pigmentation mesotherapy solution for intensive skin brightening, reducing deep-rooted pigmentation and dark spots, and improving skin elasticity and texture.
What are the key ingredients?
Tranexamoyl Dipeptide-23, Glutathione, Vitamin C, Arbutin, Niacinamide, and Sodium DNA, which inhibit tyrosinase to reduce melanin production.
How long do results last?
Over a course of 3–5 sessions at 1–2 week intervals, the anti-aging and brightening benefits are long-lasting, with effects persisting for up to 9 months.
Who should administer it?
Intended for use by certified cosmetologists and medical professionals only, via mesotherapy injection or MTS; intravascular injection is strictly prohibited.
Who manufactures SOONSU Ultra White?
It is manufactured by Cosmoderma Inc.
TOXTA 100 Units (1 Vial)
4000
$40.00
Unit price perTOXTA 100 Units (1 Vial)
4000
$40.00
Unit price perProfessional Cosmetic Treatment
TOXTA 100unit
Premium Botulinum Toxin Type A (1 Vial)
High-purity botulinum toxin formulation for cosmetic procedures and muscle relaxation treatments
JETEMA Co.
99.8% Purity
cGMP Certified
Low Resistance Risk
Professional-grade botulinum toxin for precise cosmetic applications
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Active Ingredients
- Primary Active Component
- Clostridium Botulinum Toxin Type A - high-purity formulation with exceptional potency and consistency.
- Manufacturing Standards
- Manufactured using European National Institute botulinum toxin strain, complying with cGMP standards for pharmaceutical excellence.
100 Units per Vial
High Purity 99.8%
Low Protein Content
cGMP Compliant
European Standard
Quality Assured
Treatment Benefits
-
Wrinkle Improvement
Effective reduction of mimic wrinkles and fine lines including forehead, glabella, and crow's feet -
Muscle Relaxation
Relaxation of excessive muscle contractions for smoother, more youthful appearance -
Facial Contouring
Correction of facial contours including V-line lifting through masseter muscle treatment -
Low Resistance Risk
High purity and low protein content contribute to minimal risk of developing immune resistance
Results typically visible within 5-14 days with maximum effect appearing in 1-2 weeks.
Usage Protocol
Dilution Method
Reconstitute with 0.9% sterile saline solution
Onset of Effect
5-14 days after treatment
Maximum Effect
1-2 weeks post-treatment
Duration
Up to 4 months (individual results may vary)
Treatment Areas
- Forehead lines and wrinkles
- Glabella (frown lines between eyebrows)
- Crow's feet (periorbital lines)
- Lip contour refinement
- Masseter muscle for jawline contouring
Product Specifications
| Volume | Main Use | Risk of Resistance | Duration | Treatment Area |
|---|---|---|---|---|
| 100U | Facial cosmetic procedures, fine lines, small muscle treatment | Low | Up to 4 months | Forehead, glabella, crow's feet, lip contour |
| 200U | Combined facial and larger muscle treatments | Low | Up to 4 months | Masseter muscles, trapezius, calves |
Storage & Handling
Storage Requirements — Keep sealed and store in refrigerator between 2-8°C (36-46°F) at all times.
After Reconstitution — Use immediately after preparation. If not used immediately, store in refrigerator (2-8°C) and discard after 24 hours.
Post-Treatment Precautions
- Do not press or rub the injection area to prevent toxin spreading
- Avoid smoking, drinking, sauna, and strenuous exercise for at least two weeks
- After masseter muscle treatment, avoid chewing hard foods
- Follow all post-care instructions provided by your practitioner
Product Selection Guide
Which Product is Right for Me?
Choose by considering the number of units needed for your treatment area and purpose.
TOXTA 100unit: Ideal for face-centric treatments such as fine lines, forehead wrinkles, glabella, and crow's feet. Perfect for patients seeking targeted facial rejuvenation.
TOXTA 200unit: More appropriate for combined facial and body treatments or larger muscle areas including masseter muscles, trapezius, and calves.
Frequently Asked Questions
What is TOXTA 100unit used for?
TOXTA 100unit is used for wrinkle improvement of mimic wrinkles and fine lines, muscle relaxation of excessive muscle contractions, and facial contouring including V-line lifting through masseter muscle treatment.
When does it take effect and how long does it last?
Effects are typically visible 5-14 days after treatment, with maximum effect appearing in 1-2 weeks. Results last up to 4 months (individual results may vary).
How is TOXTA 100unit diluted?
Reconstitute with 0.9% sterile saline solution. Use immediately after preparation; if not used immediately, store in refrigerator (2-8°C) and discard after 24 hours.
Who should administer TOXTA 100unit?
TOXTA 100unit should be administered by a qualified practitioner. Follow all post-care instructions provided by your practitioner.
Who manufactures TOXTA 100unit?
TOXTA 100unit is manufactured by JETEMA Co.
Rejuvenex Hydro Essence (2.5mL × 5 Syringes)
6300
$63.00
Unit price perRejuvenex Hydro Essence (2.5mL × 5 Syringes)
6300
$63.00
Unit price per
Product Identification
REJUVENEX® Hydro Essence
"Water Shine" Hydro-Lifting Booster
PharmaResearch Co., Ltd. Skin Booster (Cosmetic)
Total Volume/Content
2.5mL × 5 Syringes (Pre-filled)
Formulation Type
Transparent, viscous liquid gel (Essence)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
- c-PDRN (Cosmetic Polydeoxyribonucleotide): Hydrolyzed DNA from salmon, optimized for skin absorption to repair damaged cells.
- Sodium Hyaluronate (HA): High-quality European hyaluronic acid for intense hydration.
Mechanism of Action
A Double Effect system where HA provides immediate deep hydration and volume support, while c-PDRN penetrates the barrier to stimulate biological regeneration and collagen synthesis.
c-PDRN Hyaluronic Acid Skin Barrier Repair
Efficacy & Benefits
Main Effects
- Deep Hydration (Hydro-Lifting): Relieves inner skin dryness and provides a radiant "water glow."
- Skin Regeneration: Repairs skin barrier damaged by external irritation or aesthetic procedures (e.g., lasers).
- Texture Improvement: Softens rough skin texture and improves elasticity.
- Soothing: Calms sensitive and tired skin.
Recommended Areas
Full face (especially dry, dull skin) and Neck.
Usage Protocol
Application Method
Apply to cleansed skin. Highly recommended for use with aesthetic devices such as MTS (Microneedling), Electroporation, or Iontophoresis to enhance penetration.
Treatment Cycle
- Intensive Care: 3–5 sessions at 1–2 week intervals.
- Maintenance: 1 session every 1–2 months.
Preparation This product comes in a ready-to-use pre-filled syringe. Simply remove the cap and dispense the gel onto the skin or device head.
Series Comparison
| Product | Type | Key Feature |
|---|---|---|
| Rejuvenex Hydro | Syringe (Cosmetic) | Hydration, Glow, Daily Vitality |
| Rejuvenex Standard | Ampoule (Drug) | General Healing, Tissue Repair |
| Rejuvenex Forte | Ampoule (Drug) | Deep Scars, Ligament Repair |
Choose Hydro Essence for patients seeking immediate moisture and radiance (Water Shine) or for post-laser calming.
Storage & Handling
Storage Conditions
Room temperature (1–30°C). Store in a shaded place away from direct sunlight.
Shelf Life
36 months from the manufacturing date. Use immediately after opening.
Safety Information
Contraindications Hypersensitivity to salmon (fish) or hyaluronic acid.
Warnings For external use only (Topical Application). Avoid contact with eyes.
Common Temporary Side Effects
Mild redness or irritation may occur if used with aggressive MTS, usually subsiding within 24 hours.
Post-Treatment Care
Apply a soothing mask or moisturizer. Sun protection is essential.
Frequently Asked Questions
What is Rejuvenex Hydro Essence used for?
Rejuvenex Hydro Essence is a hydro-lifting skin booster used for deep hydration and a radiant water glow, skin barrier regeneration (including post-procedure repair), texture improvement, and soothing sensitive or tired skin.
What are the key ingredients?
The primary active ingredients are c-PDRN (Cosmetic Polydeoxyribonucleotide, hydrolyzed salmon DNA) and Sodium Hyaluronate (Hyaluronic Acid).
How is it applied?
It comes in a ready-to-use pre-filled syringe and is applied to cleansed skin. It is highly recommended for use with aesthetic devices such as MTS (Microneedling), Electroporation, or Iontophoresis. Intensive care is 3–5 sessions at 1–2 week intervals.
Who should administer Rejuvenex Hydro Essence?
It is for external (topical) use only. When combined with aesthetic devices such as MTS, Electroporation, or Iontophoresis, it should be used under professional guidance.
Who manufactures Rejuvenex Hydro Essence?
Rejuvenex Hydro Essence is manufactured by PharmaResearch Co., Ltd.
Keywords
Rejuvenex Hydro Essence c-PDRN Salmon DNA Hyaluronic Acid Skin Booster MTS Serum Water Shine Injection Korean Skincare
Kuhnthione Inj (600mg / 1200mg) (10 Vials)
4800
From $48.00
Unit price perKuhnthione Inj (600mg / 1200mg) (10 Vials)
4800
From $48.00
Unit price per
Product Identification
Kuhnthione Inj.
600mg / 1200mg
Kuhnil Biopharm Co., Ltd. Sterile Lyophilized Powder
Total Volume/Content
10 Vials per box
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technical Details
Primary Active Ingredients
Glutathione (Reduced) 600mg per vial
Key Secondary Ingredients
Sodium Bicarbonate (pH adjuster/buffer)
Mechanism of Action
Glutathione acts as a potent antioxidant, neutralizing free radicals to protect cells from oxidative stress. It conjugates with toxins in the liver for detoxification and inhibits tyrosinase enzymes to shift pigment production from eumelanin to pheomelanin.
Antioxidant Detoxification Melanin Inhibition Neuroprotection
Efficacy Summary & Expected Benefits
Main Effects and Benefits
- Neuropathy Relief: Prevention and treatment of neurological diseases caused by chemotherapy (e.g., Cisplatin).
- Skin Whitening: Brightens skin tone and reduces pigmentation such as melasma and age spots.
- Anti-Aging: Improves skin elasticity and reduces fine lines via antioxidant action.
- Liver Support: Supports liver detoxification and improves liver function parameters.
Recommended/Targeted Areas
Systemic (IV/IM) for whole-body detox and whitening; Liver support.
Usage Protocol & Application Guide
Recommended Application Method
Intravenous (IV) Injection (Drip or Slow Push) or Intramuscular (IM) Injection.
Dosage Guide
- Severe Medical Cases: 600–1200mg per day.
- Mild Cases/Maintenance: 300–600mg per day.
- Aesthetic Protocol: Typically 600mg (1 vial) to 1200mg (2 vials) per session, often mixed in 100mL saline.
Preparation Instructions
Dissolve the lyophilized powder with 5mL of Water for Injection (WFI) or Normal Saline (0.9% NaCl). Use immediately after reconstitution as potency degrades rapidly.
Dosage Strategies
| Version/Dosage | Treatment Strategy |
|---|---|
| Kuhnthione Inj. 600mg | Standard dose for general maintenance, mild detox, or initial whitening therapy. |
| Kuhnthione Inj. 1200mg | High-dose strategy for intensive whitening therapy or severe medical cases requiring higher glutathione levels. |
Storage & Handling Instructions
Required Storage Temperature
Room temperature (1°C – 30°C).
Shelf Life
36 months (3 years) from the date of manufacture.
General Handling Tips
Store in a hermetic container to prevent moisture absorption. Keep vials in the original package to protect from light exposure (Light Sensitive).
Precautions & Safety Notes
Contraindications Hypersensitivity to Glutathione.
Safety Warnings Rare cases of anaphylactoid symptoms (facial pallor, blood pressure drop) may occur; monitor patient closely. Avoid nerves and blood vessels during IM injection.
Common Temporary Side Effects
- Nausea, vomiting, loss of appetite.
- Transient rash.
Frequently Asked Questions
What is Kuhnthione Inj. used for?
Kuhnthione Inj. is used for neuropathy relief (prevention and treatment of neurological diseases caused by chemotherapy such as Cisplatin), skin whitening and reduction of pigmentation such as melasma and age spots, anti-aging, and liver detoxification support.
What is Kuhnthione Inj.'s active ingredient?
The primary active ingredient is reduced Glutathione, 600mg per vial (available in 600mg and 1200mg dosage strategies), with Sodium Bicarbonate as a pH adjuster/buffer.
How is Kuhnthione Inj. administered?
It is administered via Intravenous (IV) injection (drip or slow push) or Intramuscular (IM) injection. The lyophilized powder is first dissolved with 5mL of Water for Injection or Normal Saline (0.9% NaCl) and used immediately. Dosing is 600-1200mg per day for severe cases and 300-600mg per day for mild cases/maintenance.
Who should administer Kuhnthione Inj. and what are the precautions?
It must be administered by a medical professional. It is contraindicated in patients with hypersensitivity to Glutathione. Rare anaphylactoid symptoms (facial pallor, blood pressure drop) may occur, so monitor the patient closely, and avoid nerves and blood vessels during IM injection.
Who is the manufacturer of Kuhnthione Inj.?
Kuhnthione Inj. is manufactured by Kuhnil Biopharm Co., Ltd.
Keywords & Search Terms
Kuhnthione Kuhnil Biopharm Glutathione 600mg Skin Whitening Injection Reduced Glutathione Antioxidant IV Liver Detox Korean Whitening Shot Geontione
REJUBEAU PN Healer (2.5mL × 1 Syringe)
5500
$55.00
Unit price perREJUBEAU PN Healer (2.5mL × 1 Syringe)
5500
$55.00
Unit price per
Product Identification
REJUBEAU PN Healer
Rejubeau PN Skin Booster Series
TRACLE INC. / Rejubeau
Liquid/Gel (Pre-filled Syringe)
Total Volume/Content
2.5mL x 1 Syringe (Pre-filled)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technical Details
Primary Active Ingredients
Polynucleotide (PN) 2% (20mg/ml)
Mechanism of Action
Polynucleotide (PN), derived from salmon DNA, acts as a tissue regeneration activator. It stimulates the synthesis of collagen and elastin in the dermis (Extra Cellular Matrix restoration) and promotes angiogenesis (formation of new blood vessels) to improve skin density and thickness.
2% High Concentration PN
Optimized for Skin Regeneration
Angiogenesis Promotion
Efficacy Summary & Expected Benefits
Main Effects and Benefits
Provides comprehensive skin regeneration and wound healing by accelerating the repair of damaged skin. It improves elasticity and reduces fine lines for anti-aging, smooths skin texture while reducing pore size, and strengthens the skin barrier against environmental stress.
Recommended/Targeted Areas of Use
Full Face (General skin rejuvenation), Neck wrinkles, areas with acne scars or enlarged pores, and thin/damaged skin requiring regeneration.
Usage Protocol & Application Guide
Recommended Application Method
Intradermal Injection (Mesotherapy) or Subcutaneous Injection via
manual injection or injector gun. Recommended needle: 33G or 34G (for minimal
pain) or 30G.
Treatment Cycle/Frequency
3 to 4 sessions at 2–3 week intervals.
Maintenance recommended every 3–6 months thereafter.
Onset and Duration of Effect
Visible improvements typically appear 1–2 weeks after the first
session, with effects lasting 6–12 months.
Preparation Instructions
Ready-to-use pre-filled syringe. No dilution required.
Product Line Comparison
| Variant | Composition | Primary Focus |
|---|---|---|
| PN Healer | PN 2% | Overall regeneration, scarring, anti-aging, texture repair |
| Eye Deal | PN 1% + HA + Glutathione | Delicate eye area, dark circles, fine lines |
| Aqua Bomb | HA Focused | Intense hydration (Water glow effect) |
Use **PN Healer** for deep acne scars or severe aging concerns, and **Eye Deal** for specific under-eye treatments.
Storage & Handling Instructions
Required Storage Temperature
Room Temperature (1–30°C)
Shelf Life
24 months from the date of manufacture
General Handling Tips
Store away from direct sunlight. Do not freeze. Single-use only; discard any remaining solution.
Precautions & Safety Notes
Contraindications
Patients with known allergies to salmon or fish products (PN source), pregnancy or breastfeeding,
active infections/inflammation, or autoimmune diseases.
Safety Warnings
For professional use only by licensed medical practitioners. Avoid intravascular injection.
Common Temporary Side Effects
- "Embossing" (small raised bumps) - typically subsides within 24–48 hours
- Mild redness (Erythema), swelling, or bruising
- Mild pain or tenderness
Post-Treatment Care
- Avoid makeup for at least 6–12 hours
- Avoid saunas, steam rooms, heavy exercise, and alcohol for 3–7 days
- Apply sunscreen and moisturizer regularly
Keywords & Search Terms
REJUBEAU PN Healer
Rejubeau
Polynucleotide Injection
PN 2%
Skin Booster
Salmon DNA
Tissue Regeneration
Acne Scar Treatment
Anti-aging Injection
Korean Skin Booster
Rejuran Generic
Frequently Asked Questions
What is REJUBEAU PN Healer used for?
It provides comprehensive skin regeneration and wound healing, improving elasticity, reducing fine lines for anti-aging, smoothing skin texture while reducing pore size, and strengthening the skin barrier.
What is REJUBEAU PN Healer's key ingredient?
Its primary active ingredient is Polynucleotide (PN) 2% (20mg/ml), derived from salmon DNA.
How long do results last?
Visible improvements typically appear 1–2 weeks after the first session, with effects lasting 6–12 months. A course of 3 to 4 sessions at 2–3 week intervals is recommended.
Who should administer REJUBEAU PN Healer?
It is for professional use only and should be administered by licensed medical practitioners.
Who manufactures REJUBEAU PN Healer?
REJUBEAU PN Healer is manufactured by TRACLE INC.
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.
JBP PLAMON Inj (2mL × 10 Amps)
6100
$61.00
Unit price perJBP PLAMON Inj (2mL × 10 Amps)
6100
$61.00
Unit price per
REGENERATIVE INJECTION • PLACENTA EXTRACT
JBP PLAMON Injection
2mL x 10 Ampoules
Human placenta extract for skin regeneration, anti-aging, and overall wellness enhancement
Why KSTATION
TRUST
[MAIN PRODUCT PHOTOGRAPHY - JBP PLAMON PACKAGING AND AMPOULES]
Ingredients & Composition
ING-001
- Human Placenta Extract
- Water-soluble human placenta hydrolysis extract containing various growth factors, cytokines, and physiologically active substances that promote tissue renewal and cellular metabolism.
High Potency Medical Grade
Mechanism of Action
Activates fibroblasts, stimulates collagen production, and improves function of various organs including the liver. The extract contains essential growth factors that enhance cellular regeneration processes.
Bioactive
Key Benefits
- Promotes tissue renewal and cellular metabolism
- Stimulates natural collagen production
- Enhances liver function and organ health
- Contains essential growth factors and cytokines
[BEFORE/AFTER RESULTS AND CLINICAL EFFECTS DOCUMENTATION]
Effects & Benefits
EFF-002
Skin Regeneration
Promotes skin regeneration, reduces pigmentation, and improves elasticity through enhanced cellular renewal processes.
Proven Efficacy
Anti-Aging Properties
General anti-aging effects by neutralizing active oxygen and enhancing metabolism through enhanced cell division.
Long-term
Menopausal Support
Alleviation of symptoms associated with menopausal disorders through hormone activity enhancement.
Hormonal Balance
Fatigue Recovery
Recovery from chronic fatigue and improved overall well-being through organ function restoration.
Wellness
Usage & Application Method
USE-003
1
Preparation
Ensure sterile conditions and prepare injection site. Check ampoule integrity and allow to reach room temperature if refrigerated.
2
Administration
Administer via subcutaneous injection. Can also be used for point-by-point micro applications or with microneedling devices.
3
Treatment Cycle
Typically, one ampoule (2ml) is administered three times a week for two weeks (total of six injections).
4
Site Rotation
Change administration site each time to prevent skin induration and ensure optimal absorption.
[STEP-BY-STEP INJECTION TECHNIQUE AND SITE ROTATION GUIDE]
Target Recommendations
TRG-004
| Target Group | Symptoms/Condition | Benefits |
|---|---|---|
| Adults with Menopausal Symptoms | Hot flashes, irregular menstruation, fatigue, mood swings | Enhances female hormone activity and supports natural healing processes |
| Individuals Seeking Skin Revitalization | Pigmentation, fine lines, loss of elasticity, dull skin tone | Promotes cell division, activates fibroblasts, stimulates collagen |
| People with Chronic Fatigue | Persistent tiredness not caused by specific illness | Supports organ function restoration, particularly liver health |
Important Safety Information
Professional administration recommended for optimal safety and effectiveness. Important precautions to ensure safe usage:
- Not for individuals with known hypersensitivity to the drug
- Contraindicated for those with organic diseases
- Not suitable for newborns/premature infants due to benzyl alcohol content
- Handle glass ampoules carefully to prevent glass fragment contamination
- Maintain sterile technique throughout administration
- Monitor for any adverse reactions during treatment
Storage & Handling
STG-005
Storage Requirements
- Temperature: Store at room temperature 1-30°C
- Light Protection: Keep in light-resistant, sealed container
- Freezing: Do not freeze
- Container: Maintain original sealed packaging
Handling Precautions
- Open glass ampoules carefully to minimize risk of contamination
- Use immediately after opening
- Ensure sterile technique during handling
- Dispose of used ampoules according to medical waste guidelines
[PROPER STORAGE CONDITIONS AND HANDLING SAFETY GUIDELINES]
Product Specifications
SPC-006
- Product Name
- JBP PLAMON injection
- Volume per Ampoule
- 2mL
- Package Contents
- 10 Ampoules per box
- Active Ingredient
- Human Placenta Extract
- Administration Route
- Subcutaneous injection / Topical with microneedling
- Recommended Course
- 6 injections over 2 weeks (3x per week)
[PROFESSIONAL CERTIFICATION AND QUALITY ASSURANCE DOCUMENTATION]
Frequently Asked Questions
FAQ-007
- What is JBP PLAMON injection used for?
- JBP PLAMON injection is a human placenta extract used for skin regeneration and anti-aging, alleviation of menopausal disorder symptoms, and recovery from chronic fatigue. It promotes tissue renewal, stimulates collagen production, and supports organ function including the liver.
- What is JBP PLAMON's active ingredient?
- The active ingredient is Human Placenta Extract — a water-soluble human placenta hydrolysis extract containing growth factors, cytokines, and physiologically active substances. Each box contains 10 ampoules of 2mL each.
- How is JBP PLAMON administered?
- It is administered via subcutaneous injection, and can also be used for point-by-point micro applications or with microneedling devices. The typical course is one 2mL ampoule three times a week for two weeks (six injections total), rotating the administration site each time.
- Who should administer JBP PLAMON and what are the precautions?
- Professional administration is recommended. It is contraindicated for individuals with known hypersensitivity to the drug or with organic diseases, and is not suitable for newborns or premature infants due to benzyl alcohol content. Sterile technique must be maintained and glass ampoules handled carefully to prevent glass fragment contamination.
Kamomis 100 Units (1 Vial)
3000
$30.00
Unit price perKamomis 100 Units (1 Vial)
3000
$30.00
Unit price per
Botulinum Toxin Hugel Co., Ltd. Professional Grade
Advanced Cosmetic Injectable
Kamomis
100 Units / 1 Vial
Professional-grade Botulinum Toxin Type A for temporary improvement of moderate to severe glabellar lines
#WrinkleImprovement #GlabellarLines #MuscleRelaxation #AntiAging
Kamomis 100U Product Visualization
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Active Ingredients and Composition
Highly purified and stable Botulinum Toxin Type A formulation in lyophilized powder form for optimal stability and efficacy.
Botulinum Toxin Type A
Primary active ingredient derived from Clostridium Botulinum
100 Units
Lyophilized Powder Form
Ensures long-term stability when stored correctly
StabilizedBotulinum Toxin Mechanism of Action Diagram
💡 Benefits and Functions
Glabellar Line Improvement
Temporary improvement of moderate to severe frown lines
Muscle Relaxation
Relaxation of corrugator and procerus muscles
Quick Onset
Effects begin within 2-3 days of treatment
Long Duration
Results last approximately 3 to 4 months
Fast Acting Long Lasting Professional Use Proven Results
Key Benefits
- Temporary improvement of moderate to severe glabellar lines
- Precise muscle relaxation for natural-looking results
- Refreshed and more youthful appearance
- Professional-grade formulation for optimal efficacy
Before and After Glabella Treatment Results
Kamomis 100U works by temporarily blocking nerve signals to the injected muscles, leading to their relaxation and the smoothing of associated wrinkles for a natural, refreshed appearance.
🧪 Usage Protocol and Application
1
Reconstitution
Reconstitute with sterile saline: 2.5ml for 4U/0.1ml concentration or 1.25ml for 8U/0.1ml concentration
Reconstitute with sterile saline: 2.5ml for 4U/0.1ml concentration or 1.25ml for 8U/0.1ml concentration
2
Dosage Preparation
Prepare total dose of 20U for glabellar lines treatment
Prepare total dose of 20U for glabellar lines treatment
3
Injection Technique
Administer as five 4U injections into corrugator and procerus muscles
Administer as five 4U injections into corrugator and procerus muscles
4
Precise Targeting
Ensure precise injection into target muscles for optimal results
Ensure precise injection into target muscles for optimal results
5
Post-Treatment
Monitor patient and provide appropriate aftercare instructions
Monitor patient and provide appropriate aftercare instructions
After reconstitution, store refrigerated at 2-8°C and use within 24 hours; discard any remaining solution. For professional use only by qualified medical practitioners.
Glabellar Lines Treatment Map and Injection Guide
📊 Product Specifications
100U Units per Vial
2-3 Days Onset
3-4 Months Duration
Content
100 units / vial
Manufacturer
Hugel, Co., Ltd.
Form
Lyophilized powder
Onset Time
2-3 days (maximum effect at 1-2 weeks)
Duration
Approximately 3 to 4 months
Recommended Dose
20U total for glabellar lines (5 × 4U injections)
⚠️ Important Safety Information
For professional use only. Must be administered by qualified medical practitioners with appropriate training in cosmetic injection procedures.
- Store in refrigerator at 2-8°C
- Do not freeze the product
- After reconstitution, store at 2-8°C and use within 24 hours
- Discard any remaining solution after use
- Do not use if vial appears damaged
Contraindications and Precautions
- Not for use in patients with known hypersensitivity to botulinum toxin
- Avoid use in presence of infection at injection site
- Use with caution in patients with neuromuscular disorders
- Proper injection technique essential to avoid complications
Storage and Handling
- Refrigerated storage required at 2-8°C
- Protect from light and moisture
- Check expiration date before use
- Follow proper sterile technique during preparation
Storage and Safety Guidelines Infographic
❓ Frequently Asked Questions
A. Standard dilution varies based on patient needs and treatment area. Typically 2.5ml of 0.9% sterile saline to achieve 4U/0.1ml concentration, or 1.25ml for 8U/0.1ml concentration. A. Effects generally last for approximately 3 to 4 months. Onset of action is typically observed within 2-3 days, with maximum effect reached at 1-2 weeks. A. For glabellar lines, the recommended total dose is 20U, administered as five 4U injections into the corrugator and procerus muscles. A. Store in a refrigerator at 2-8°C. Do not freeze the product. Do not use if the vial appears damaged. After reconstitution, store at 2-8°C and use within 24 hours. A. Kamomis 100U is for professional use only and should be administered by a qualified medical practitioner with appropriate training in cosmetic injection procedures.
Q. What is the recommended dilution for Kamomis 100U?
Q. How long do the effects of Kamomis 100U last?
Q. What is the recommended dose for glabellar lines?
Q. How should Kamomis 100U be stored?
Q. Who can administer Kamomis 100U?