100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
COLLECTION
Nutritional and Antioxidant Wellness
Boost your well-being from the inside out with our nutritional and antioxidant wellness products. This collection provides the essential support your body needs to fight oxidative stress and maintain a healthy, vibrant appearance.
27 products
27 products
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Detoxione Inj 1200mg
6200
$62.00
Unit price perDetoxione Inj 1200mg
6200
$62.00
Unit price perProfessional Vitamin Injection
DETOXIONE inj 1200mg
10 Vials per Box
Advanced glutathione injection solution for powerful antioxidant support and skin brightening benefits
PROFESSIONAL GRADE 1200mg GLUTATHIONE ANTIOXIDANT POWER
Each vial contains 1200mg of reduced glutathione in freeze-dried (lyophilized) porous white solid form
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Active Ingredients
- Primary Active Component
- Glutathione (Reduced) - A powerful tripeptide antioxidant with low molecular weight for optimal bioavailability and cellular protection.
Glutathione 1200mg Reduced Form Low Molecular Weight
- Mechanism of Action
- Neutralizes free radicals, inhibits tyrosinase enzyme to suppress melanin production, and supports liver detoxification processes for comprehensive antioxidant benefits.
-
Antioxidant Network
Critical component of the body's antioxidant system, protecting cells from oxidative stress damage. -
Melanin Suppression
Inhibits tyrosinase enzyme activity to reduce melanin production for skin brightening effects. -
Liver Support
Plays key role in liver detoxification processes and various metabolic reactions.
Expected Benefits
- Skin brightening and improved skin tone
- Powerful antioxidant protection against free radicals
- Enhanced liver detoxification processes
- Anti-aging benefits by combating oxidative stress
Skin Brightening Detoxification Anti-aging
Glutathione's antioxidant properties extend beyond skin brightening to support DNA repair and protein synthesis.
Usage Protocol
Professional Administration
Must be administered by licensed healthcare professional only - do not self-administer
Must be administered by licensed healthcare professional only - do not self-administer
Dosage Determination
Healthcare provider will determine appropriate dosage based on individual needs and treatment goals
Healthcare provider will determine appropriate dosage based on individual needs and treatment goals
Reconstitution Before Use
Supplied as a freeze-dried (lyophilized) porous white solid and must be reconstituted with sterile water for injection or normal saline before administration
Supplied as a freeze-dried (lyophilized) porous white solid and must be reconstituted with sterile water for injection or normal saline before administration
Injection Method
Administered via intramuscular or intravenous injection using sterile technique
Administered via intramuscular or intravenous injection using sterile technique
Treatment Monitoring
Follow-up with healthcare provider to monitor progress and adjust treatment as needed
Follow-up with healthcare provider to monitor progress and adjust treatment as needed
Severe Cases
600-1200mg daily (as determined by healthcare professional)
Maintenance/Mild Cases
300-600mg daily (as determined by healthcare professional)
Administration Routes
Intramuscular or Intravenous injection
Professional Use Only - This product is for professional use and should only be administered by a licensed healthcare professional.
Combination Therapy
- Enhanced Efficacy with Vitamin C
- Glutathione efficacy can be significantly enhanced when used in combination with Vitamin C, which helps regenerate reduced glutathione and boosts antioxidant power.
- Synergistic Combinations
- Often combined with Thioctic Acid and other complementary ingredients to maximize skin brightening and antioxidant benefits.
Product Specifications
| Component | Specification | Form | Administration |
|---|---|---|---|
| Glutathione (Reduced) | 1200mg per vial | Freeze-dried (lyophilized) porous white solid | IM/IV injection |
| Package Size | 10 vials per box | Individual vials | Professional use |
Safety & Storage
Professional Administration Required - This product must only be administered by a licensed healthcare professional.
Contraindications - Do not use if allergic to glutathione or any inactive ingredients. Inform your doctor if you have asthma, are pregnant, or breastfeeding.
After Reconstitution - Per the manufacturer's labeling, the reconstituted solution should be used immediately. Storing reconstituted product is not recommended.
Storage Temperature
Room temperature (1-30°C), before reconstitution
Storage Container
Sealed container
Professional Use
Licensed healthcare provider only
Side Effects
Possible injection site reactions
Product Classification
| Purpose | Key Ingredient | Expected Efficacy | Recommended Combinations | Method |
|---|---|---|---|---|
| Skin Brightening & Antioxidant | Glutathione 1200mg | Melanin suppression, skin brightening, antioxidant benefits, liver detoxification | Vitamin C, Thioctic Acid | IV injection |
Who is this product right for?
If your primary goal is to achieve brighter and more even skin tone while benefiting from strong antioxidant and detoxification support, this product is well-suited for you. For enhanced skin-brightening effects, consider combining it with Vitamin C under professional guidance.
Frequently Asked Questions
What is DETOXIONE inj 1200mg used for?
DETOXIONE inj 1200mg is used for skin brightening and improved skin tone, powerful antioxidant protection against free radicals, enhanced liver detoxification, and anti-aging benefits by combating oxidative stress.
What is DETOXIONE's active ingredient?
The active ingredient is reduced Glutathione, 1200mg per vial - a powerful tripeptide antioxidant with low molecular weight for optimal bioavailability and cellular protection.
How is DETOXIONE administered?
DETOXIONE is administered via intramuscular or intravenous injection using sterile technique. Before use it is reconstituted with sterile water for injection or normal saline, and the reconstituted solution should be used immediately. Dosing is 600-1200mg daily for severe cases or 300-600mg daily for maintenance, as determined by a healthcare professional.
Who should administer DETOXIONE and what are the precautions?
DETOXIONE must only be administered by a licensed healthcare professional. Do not use if allergic to glutathione or any inactive ingredients. Inform your doctor if you have asthma, are pregnant, or breastfeeding.
VITAMIN C Inj (20mL × 10 Vials)
3800
$38.00
Unit price perVITAMIN C Inj (20mL × 10 Vials)
3800
$38.00
Unit price perVITAMIN C Injection
20mL × 10 Vials
Ascorbic Acid Injection
Ascorbic acid injection, 10g per 20mL vial, 10 vials per box. A prescription medicine for administration by a healthcare professional.
Main Product Image - Vitamin C Injection Vials
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Premium Quality
Vitamin C Injection 10g
This package contains 10 vials, each with 20mL of ascorbic acid solution (10g per vial), for professional clinical use.
Active Ingredients & Formulation
- Ascorbic Acid (Vitamin C)
- 10g/20mL Ascorbic acid (vitamin C), 10g per 20mL vial (500mg/mL).
Ingredient Mechanism Diagram - Vitamin C Pathways
Usage Protocol & Administration
1
Professional Assessment
Consultation with qualified medical professional to determine appropriate dosage and treatment plan based on individual needs.
2
Dilution Preparation
The solution must be properly diluted before intravenous administration. Never administer undiluted.
3
Administration Method
Can be administered via intravenous (IV) or intramuscular (IM) injection in clinical setting only.
4
Treatment Cycle
For severe deficiency: 500mg to 1g daily. Otherwise as determined by the treating physician.
Administration Guide Visual
Product Specifications
| Attribute | Specification | Details |
|---|---|---|
| Active Ingredient | Ascorbic Acid | 10g per 20mL vial |
| Package Contents | 10 Vials | 20mL each vial |
| Administration | IV/IM Injection | Clinical setting required |
| Storage Temperature | 2°C - 8°C | Light-resistant container |
| Shelf Life | Use within 4 hours | After vial puncture |
Storage & Handling Requirements
Store in light-resistant, hermetic container between 2°C and 8°C. The solution is preservative-free. Once the vial is punctured, any unused portion must be discarded within 4 hours to prevent microbial contamination.
Safety Information & Precautions
Important Safety Guidelines
This product must be diluted before intravenous administration and requires prescription use in clinical settings only.
- Do not administer undiluted
- High doses may cause gastrointestinal discomfort
- May affect urine acidity levels
- Professional medical supervision required
Contraindications
Use with caution in patients with renal impairment, history of kidney stones, or certain genetic disorders. Should not be administered to patients with hyperoxaluria. Consult medical professional before use if pregnant, breastfeeding, or taking other medications.
Frequently Asked Questions
What is VITAMIN C Injection used for?
VITAMIN C Injection is an ascorbic acid injection for use by a healthcare professional. Its use is determined by the treating physician; KSTATION does not make treatment claims.
What is VITAMIN C Injection's active ingredient?
The active ingredient is Ascorbic Acid (Vitamin C), 10g per 20mL vial.
How is VITAMIN C Injection administered?
It is administered via intravenous (IV) or intramuscular (IM) injection in a clinical setting. The solution must be properly diluted before intravenous administration and never given undiluted. For severe deficiency, 500mg to 1g daily; for skin and antioxidant benefits, as determined by a medical professional.
Who should administer VITAMIN C Injection and what are the precautions?
It requires professional medical supervision in clinical settings. Use with caution in patients with renal impairment, history of kidney stones, or certain genetic disorders. It should not be administered to patients with hyperoxaluria. Consult a medical professional before use if pregnant, breastfeeding, or taking other medications.
CINDELLA Inj (5mL × 10 Amps)
3150
$31.50
Unit price perCINDELLA Inj (5mL × 10 Amps)
3150
$31.50
Unit price per
Injectable DAEHAN NEW PHARM Antioxidant
Professional Anti-Aging Solution
CINDELLA
Injection [I.V.]
5mL x 10 Ampoules
Alpha-Lipoic Acid injection for comprehensive anti-aging and skin brightening through powerful antioxidant action
#SkinBrightening #AntiAging #Detoxification #FatigueRecovery
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Key Ingredients and Formulation
CINDELLA contains Thioctic Acid (Alpha-Lipoic Acid) in a sterile injectable solution formulated for professional administration.
Thioctic Acid (Alpha-Lipoic Acid)
Powerful antioxidant that neutralizes free radicals and boosts cellular metabolism
25mg/5mLMechanism of Action
As a coenzyme vital for cellular energy metabolism, Thioctic Acid operates in both water-soluble and fat-soluble domains within the body, making it more comprehensive than Vitamins C and E. It promotes glucose utilization, helps convert carbohydrates into energy, and prevents glycation of collagen - a key contributor to skin aging.
Antioxidant Action
Neutralizes free radicals and enhances effects of Vitamins C and E
Melanin Suppression
Helps suppress melanin production for skin brightening
Cellular Metabolism
Boosts cellular energy production and metabolism
💡 Expected Benefits and Effects
Anti-Aging Effects
Reduction of fine lines and prevention of collagen glycation
Skin Brightening
Brighter, more even skin tone with reduced hyperpigmentation
Enhanced Antioxidant Defense
Comprehensive protection and detoxification support
Improved Skin Texture
Enhanced skin elasticity and overall texture improvement
Energy & Vitality
Fatigue recovery and increased energy levels
Whitening Anti-Aging Detoxification Energy Boost
Comprehensive Benefits
- Neutralizes harmful free radicals throughout the body
- Enhances the antioxidant effects of other vitamins and nutrients
- Supports cellular energy metabolism and glucose utilization
- Helps prevent conversion of proteins into toxic sugar-derived substances
- Contributes to overall skin health, tone, and radiance
The synergistic effects of Thioctic Acid provide sustained improvements in skin quality and overall vitality when administered as part of a comprehensive treatment protocol.
🧪 Usage Protocol and Administration
Professional Use Only
This product must be administered by a certified medical professional via intravenous injection only.
1
Initial Treatment Phase
Administer once weekly for 10 treatment sessions
Administer once weekly for 10 treatment sessions
2
Maintenance Phase
Reduce frequency to once every 2 weeks or once monthly
Reduce frequency to once every 2 weeks or once monthly
3
Combination Protocol
Often combined with Glutathione and Vitamin C for enhanced effects
Often combined with Glutathione and Vitamin C for enhanced effects
Cinderella Injection Protocol
CINDELLA is often used as part of a "Cinderella Injection" or "Health Cocktail" protocol, combining Thioctic Acid with complementary ingredients for maximum skin whitening and anti-aging benefits.
Treatment Cycle
10 sessions (weekly) + maintenance protocol
Administration
Intravenous infusion by medical professional
Combination
Often paired with Glutathione and Vitamin C
📊 Product Specifications
5mL Per Ampoule
10 Ampoules/Box
25mg Active Ingredient
| Specification | Details |
|---|---|
| Active Ingredient | Thioctic Acid (Alpha-Lipoic Acid) 25mg/5mL |
| Formulation | Injectable liquid in brown ampoule |
| Package Contents | 10 ampoules × 5mL per box |
| Administration | Intravenous injection by medical professional |
| Storage Temperature | 1-30°C (room temperature), light-protected sealed container |
| Shelf Life | 36 months from manufacturing date |
⚠️ Important Safety Information
Professional use only. Must be administered by certified medical professionals. Proper storage and handling required.
- Store in sealed condition at room temperature (1-30°C)
- Professional administration required via IV infusion
- Keep out of reach of children
- Use only as directed by healthcare provider
Contraindications and Precautions
- Do not use if pregnant or breastfeeding
- Consult doctor before use if you have pre-existing medical conditions
- Check for medication interactions before treatment
- Open ampoules with caution to prevent glass contamination
Storage and Handling Instructions
- Store at room temperature between 1-30°C
- Keep in original sealed packaging until use
- Protect from direct sunlight and extreme temperatures
- Use within shelf life: 36 months from manufacturing date
❓ Frequently Asked Questions
A. CINDELLA is used for anti-aging, skin brightening, enhanced antioxidant defense, improved skin texture, and energy and vitality through fatigue recovery, via the action of Thioctic Acid (Alpha-Lipoic Acid). A. The active ingredient is Thioctic Acid (Alpha-Lipoic Acid), 25mg per 5mL ampoule - a powerful antioxidant that operates in both water-soluble and fat-soluble domains and boosts cellular metabolism. A. CINDELLA is administered by a certified medical professional via intravenous injection. The typical protocol is once weekly for 10 sessions, followed by maintenance every 2 weeks or monthly. A. CINDELLA must be administered by a certified medical professional. Do not use if pregnant or breastfeeding, consult a doctor if you have pre-existing conditions, and check for medication interactions before treatment. A. CINDELLA is manufactured by DAEHAN NEW PHARM. A. CINDELLA contains Thioctic Acid (Alpha-Lipoic Acid), which operates in both water-soluble and fat-soluble domains, making it more comprehensive than Vitamins C and E alone. It also helps prevent collagen glycation, a key factor in skin aging. A. The typical protocol involves 10 weekly sessions for the initial treatment phase, followed by maintenance sessions every 2 weeks or monthly as recommended by your healthcare provider. A. Yes, CINDELLA is often used as part of a "Cinderella Injection" protocol, combined with Glutathione and Vitamin C for enhanced skin whitening and antioxidant effects. Consult your provider for optimal combinations. A. Expected benefits include anti-aging effects, brighter and more even skin tone, enhanced antioxidant defense, improved skin elasticity, and increased energy levels through better cellular metabolism. A. Store CINDELLA in its original sealed packaging at room temperature between 1-30°C, away from direct sunlight. The product has a shelf life of 36 months from the manufacturing date.
Q. What is CINDELLA used for?
Q. What is CINDELLA's active ingredient?
Q. How is CINDELLA administered?
Q. Who should administer CINDELLA and what are the precautions?
Q. Who is the manufacturer of CINDELLA?
Q. What makes CINDELLA different from other antioxidant treatments?
Q. What is the recommended treatment schedule?
Q. Can CINDELLA be combined with other treatments?
Q. What are the expected benefits of CINDELLA treatment?
Q. How should CINDELLA be stored?
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
DAIHAN Isotonic Sodium Chloride Saline Inj (20mL × 50 Amps)
5500
$55.00
Unit price perDAIHAN Isotonic Sodium Chloride Saline Inj (20mL × 50 Amps)
5500
$55.00
Unit price perMedical Grade Injectable
DAIHAN Isotonic Sodium Chloride Injection
20mL × 50 Ampoules
Professional-grade sterile diluent and electrolyte replacement solution
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧩 Essential Information
Core Value Proposition
Premium quality isotonic sodium chloride injection designed for professional medical and aesthetic applications. This sterile, non-pyrogenic solution serves dual purposes as an effective electrolyte replacement therapy and a reliable diluent for various injectable preparations. With balanced osmolarity matching human plasma, it ensures optimal safety and compatibility.
Active Ingredient
0.9%
Sodium Chloride
9mg/mL isotonic concentration
Volume
20
mL per ampoule
Osmolarity
308
mOsmol/L
Similar to blood plasma
Package Size
50
Glass Ampoules
📋 Detailed Specifications
| Specification Category | Details/Values | Additional Information |
|---|---|---|
| Physical Properties | Clear, colorless solution | Sterile and non-pyrogenic |
| Chemical Composition | Sodium Chloride 0.9% | Medical grade purity |
| Osmolarity | 308 mOsmol/L | Isotonic with human plasma |
| Storage Requirements | Below 30°C, protect from freezing | Hermetic container required |
| Administration Method | I.V., S.C., or Rectal | Professional supervision required |
| Dosage Range | 20mL ~ 1000mL | Based on physician's instructions |
🧬 Mechanism of Action
Electrolyte ReplenishmentProvides essential sodium and chloride ions to maintain proper fluid balance and cellular function in the body.Isotonic PropertiesMatches the osmolarity of blood plasma (approximately 308 mOsmol/L), preventing osmotic shock and ensuring safe administration.Diluent FunctionServes as a sterile vehicle for reconstituting powder medications or adjusting concentrations of liquid formulations.Fluid Balance MaintenanceHelps restore and maintain proper hydration levels while supporting normal physiological processes.
💡 Clinical Applications & Benefits
Primary Medical Applications
Essential for fluid and electrolyte replacement therapy in clinical settings. Widely used for treating mild dehydration, electrolyte imbalances, and as a foundation for various therapeutic protocols.
Electrolyte Replacement Fluid Therapy Dehydration Treatment
Professional Diluent Use
Serves as the gold standard diluent for aesthetic and wellness applications, ensuring safe dilution of active compounds while maintaining stability and sterility.
- Vitamin injection preparation and dilution
- Antioxidant compound mixing (Glutathione, Vitamin C)
- Custom aesthetic cocktail preparation
- Powder medication reconstitution
Safety & Compatibility
Demonstrated excellent compatibility with a wide range of injectable substances while maintaining the highest safety standards for professional use.
🧪 Professional Usage Protocol
1
Pre-Application Inspection
Carefully inspect each ampoule for cracks, discoloration, or precipitate. Ensure the solution remains clear and colorless before use. Check expiration date and storage conditions.
2
Aseptic Preparation
Use proper aseptic technique when opening glass ampoules. Take precautions to prevent glass particle contamination during the breaking process.
3
Administration or Dilution
For direct use: administer via I.V., S.C., or rectal route as prescribed. For dilution: follow manufacturer's instructions for specific medications being mixed.
4
Post-Use Protocol
Discard any unused portion immediately after opening. Do not store opened ampoules. Proper disposal of glass ampoules according to medical waste guidelines.
Critical Safety Information
This product is for professional use only and requires proper medical supervision. Ensure compliance with all safety protocols for optimal patient outcomes.
- Do not use if solution is discolored, cloudy, or contains precipitate
- Store in hermetic container at temperatures not exceeding 30°C
- Contraindicated in patients with hypernatremia or fluid overload
- Use with caution in congestive heart failure or renal impairment
- Handle glass ampoules carefully to prevent contamination
- Discard unused portion immediately after opening
✅ Quality Assurance & Standards
Medical Grade
Certified
Pharmaceutical
Sterility
Guaranteed
Non-pyrogenic
Purity
USP
Standard
Compliance
International
Standards
Manufacturing Excellence
Produced under strict pharmaceutical manufacturing conditions with comprehensive quality control testing. Each batch undergoes rigorous sterility, purity, and potency testing to ensure consistent therapeutic efficacy.
📄 Complete Product Information
Package Contents50 sterile glass ampoules, each containing 20mL of 0.9% Sodium Chloride solution, packaged in protective cartons with individual ampoule sleeves.Storage & HandlingStore at room temperature (below 30°C) in original packaging. Protect from freezing and direct sunlight. Use aseptic technique for handling.Professional ConsultationRecommended for use by qualified healthcare professionals familiar with injection techniques and sterile preparation methods.CompatibilityCompatible with most injectable medications. Verify compatibility with specific drugs before mixing. Consult pharmaceutical references for detailed compatibility information.
❓ Frequently Asked Questions
What is DAIHAN Isotonic Sodium Chloride Injection used for?
It is used as a sterile diluent for reconstituting powder medications and adjusting concentrations of liquid formulations, and as an electrolyte replacement and fluid therapy solution. As a diluent it is commonly used for vitamin injection preparation, antioxidant compound mixing (Glutathione, Vitamin C), and custom aesthetic cocktail preparation.
What is the active ingredient in DAIHAN Sodium Chloride Injection?
The active ingredient is Sodium Chloride 0.9% (9mg/mL), an isotonic concentration with an osmolarity of 308 mOsmol/L, similar to human blood plasma.
How is DAIHAN Sodium Chloride Injection used as a diluent or administered?
As a diluent, it serves as a sterile vehicle for reconstituting powder medications; follow the manufacturer's instructions for the specific medication being mixed. For direct use, it is administered via I.V., S.C., or rectal route, with a dosage range of 20mL to 1000mL based on physician's instructions.
Who should administer it and what are the precautions?
It is for professional use only and requires medical supervision by qualified healthcare professionals. Do not use if the solution is discolored, cloudy, or contains precipitate. It is contraindicated in patients with hypernatremia or fluid overload, and should be used with caution in congestive heart failure or renal impairment. Discard any unused portion immediately after opening.
VELATOX GF11 (3mL x 5 Vials)
6900
$69.00
Unit price perVELATOX GF11 (3mL x 5 Vials)
6900
$69.00
Unit price perVELATOX GF11 Premium Skin Booster
Dual Solution System for Complete Skin Revitalization
11 Growth Factors
Multi-Peptide Complex
Antioxidant Vitamins
Anti-Aging
Skin Regeneration
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
VELATOX GF11 is a comprehensive dual solution system designed for professional skin rejuvenation. Combining the power of VELATOX (3mL x 5 Vials) intensive treatment solution with VELASEM (10mL x 2 Vials) post-care solution, this premium skin booster delivers exceptional anti-aging, regeneration, and brightening results.
Key Ingredients & Formulation
🔬 VELATOX Solution (3mL x 5 Vials)
11 Cell Growth Factors
- EGF (Epidermal Growth Factor) - Promotes skin cell regeneration
- FGF (Fibroblast Growth Factor) - Stimulates collagen production
- IGF (Insulin-like Growth Factor) - Enhances cellular metabolism
- Plus 8 additional growth factors for comprehensive skin renewal
Multi-Peptide Complex
- Acetyl Hexapeptide-8 - Synthetic hexapeptide (INCI: Acetyl Hexapeptide-8)
- Palmitoyl Pentapeptide-4 - Stimulates collagen and elastin synthesis
- Palmitoyl Tetrapeptide-7 - Anti-inflammatory properties
- Nicotinoyl Tripeptide-1 - Improves skin tone and texture
- Dipeptide Diaminobutyroyl Benzylamide - Synthetic dipeptide
Antioxidant Vitamin Complex
- Vitamin C - Brightening and antioxidant protection
- Vitamin B2 - Skin cell energy metabolism
- Vitamin B3 (Niacinamide) - Pore refinement and barrier strengthening
- Vitamin B12 - Anti-inflammatory and regenerative
Additional Active Ingredients
- Adenosine - Wrinkle improvement
- Arbutin - Melanin synthesis inhibition
- L-Carnitine - Cellular energy production
💧 VELASEM After-Treatment Solution (10mL x 2 Vials)
- Arbutin - Anti-pigmentation and whitening
- Moisturizing Complex - Intense hydration and soothing
- Antibacterial Components - Post-treatment protection
Expected Efficacy & Benefits
🎯 Intense Anti-Aging & Wrinkle Reduction
Promotes collagen and elastin regeneration through 11 Growth Factors and peptides, visibly reducing wrinkles, fine lines, and expression lines for smoother, younger-looking skin.
✨ Antioxidant Protection & Anti-Pigmentation
Powerful antioxidant vitamins neutralize free radicals to prevent premature aging. Arbutin works to suppress melanin production, resulting in a brighter, more even complexion.
🔄 Skin Regeneration & Barrier Reinforcement
Accelerates the skin's natural renewal process by supporting cell growth and strengthening the skin barrier. Particularly beneficial for faster recovery after cosmetic procedures.
💪 Elasticity and Firmness
Significantly improves overall skin elasticity and firmness, delivering a lifted, more youthful appearance with enhanced skin density.
🛡️ Anti-Inflammatory Action
Decreases inflammation that can impede the skin's natural regeneration process, creating optimal conditions for healing and rejuvenation.
Treatment Protocol & Usage Guide
Recommended Treatment Cycle: 3-5 sessions at intervals of once every two weeks
📍 Treatment Areas
💉 VELATOX Application Method
- Application Technique: Professional application via MTS (Microneedling Therapy System), nano-needles, or direct micro-injection
- Dosage: Do not exceed 0.1-0.2mL per application point
-
Needle Depth Guidelines:
- Forehead: 0.2~0.5mm
- Cheeks: 0.2~0.5mm
- Neck: 0.2~0.7mm
- Eye area: Adjust carefully based on skin thickness
- Important: Do not mix with other solutions to maintain efficacy
🌟 VELASEM Post-Treatment Application
- Application Timing: Immediately after VELATOX procedure
- Application Method: Spray 3-5 times on the face OR apply evenly as serum and gently tap to absorb
- Alternative Method: Use with airbrush for even distribution
- Purpose: Provides immediate soothing, hydration, and anti-pigmentation benefits to maximize treatment results
Product Comparison & Selection Guide
| Product Name | Key Ingredients | Treatment Areas | Skin Type | Main Efficacy |
|---|---|---|---|---|
| VELATOX GF11 | 11 GF, Multi-Peptides, Vitamin Complex | Entire face, Neck, Eye area | All Skin Types | Regeneration, Anti-aging, Brightening, Elasticity |
| VELASEM (Aftercare) | Anti-Pigmentation, Moisturizing Factors | Entire face, Treated areas | All Skin Types | Soothing, Anti-Pigmentation, Hydration |
Which Product Is Right for Me?
VELATOX GF11 is designed as a comprehensive skin revitalization solution, perfect for individuals seeking all-in-one anti-aging, elasticity, and brightening effects. The dual system ensures not only deep revitalization with VELATOX but also provides essential aftercare, soothing, and anti-pigmentation benefits with VELASEM.
Storage Conditions & Precautions
📦 Storage Requirements
- Unopened Product: Store in a cool, dry place between 1°C - 30°C, away from direct sunlight
- After Opening: Must be refrigerated between 5°C - 15°C and used within 15 days (two weeks)
⚠️ Important Precautions
- Professional Use Only: This product should only be administered by trained professionals
- Do Not Mix: Do not mix VELATOX with other solutions to maintain optimal efficacy
- Skin Condition: Not recommended for use on sensitive, irritated, or wounded skin
- Post-Treatment Care: Avoid excessive massaging of the treated area after application
- Consultation Required: Proper consultation and assessment should be performed before treatment
Product Specifications
Product Name
VELATOX GF11 Premium Skin Booster (Dual Solution System)
Package Contents
VELATOX (3mL x 5 Vials) + VELASEM (10mL x 2 Vials)
Formulation Type
VELATOX: Ampoule type for injection/microneedling
VELASEM: Spray/Serum type for topical application
Recommended Treatment Cycle
3-5 sessions at intervals of once every two weeks
Suitable Skin Types
All skin types seeking anti-aging, regeneration, and brightening effects
Product Tags & Keywords
Skin booster, Cell Growth Factor, EGF, FGF, IGF, Peptide, Acetyl Hexapeptide-8, Antioxidant Vitamin, Anti-aging, Wrinkle Reduction, Elasticity, Brightening, Skin Regeneration, Post-treatment care, Microneedling ampoule, Multi-shot, VELASEM, Professional skin treatment, Collagen boosting, Premium aesthetic solution
Frequently Asked Questions
What is VELATOX GF11 used for?
It is a dual solution system for professional skin rejuvenation, delivering intense anti-aging and wrinkle reduction, antioxidant protection and anti-pigmentation, skin regeneration and barrier reinforcement, elasticity and firmness, and anti-inflammatory action.
What is VELATOX GF11's key ingredient?
The VELATOX solution contains 11 Cell Growth Factors (including EGF, FGF, and IGF), a Multi-Peptide Complex (such as Acetyl Hexapeptide-8), an Antioxidant Vitamin Complex (Vitamin C, B2, B3, B12), plus Adenosine, Arbutin, and L-Carnitine.
How long do results last?
A recommended treatment cycle is 3-5 sessions at intervals of once every two weeks.
Who should administer VELATOX GF11?
It should only be administered by trained professionals, with proper consultation and assessment performed before treatment.
LAENNEC Inj (2mL × 10 / 50 Vials)
9700
From $97.00
Unit price perLAENNEC Inj (2mL × 10 / 50 Vials)
9700
From $97.00
Unit price per2mL × 10 or 50 per Box
Laennec inj.
Human Placenta Hydrolysate Injection
Human placenta hydrolysate injection, licensed in Korea as a prescription medicine for the improvement of liver function in chronic liver disease.
Packaging Update: Ampoule to Vial
The manufacturer is changing LAENNEC from glass ampoules to vials (new packaging released by the manufacturer in August 2026). Until existing ampoule stock is used up, your order may ship in either format, and a single order may include both.
According to the manufacturer, only the container has changed. The ingredient, 2mL volume per unit, and approved indications are the same for both formats.
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
Licensed Prescription Injection
LAENNEC inj contains 112mg of water-soluble Human Placenta Hydrolysate per 2mL ampoule, a hydrolysate containing amino acids, peptides and other placenta-derived components.
- Licensed indication: improvement of liver function in chronic liver disease
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 derived from human placenta.
- Growth Factors
- Natural Complex Protein components of the hydrolysate.
- Amino Acids & Peptides
- Complete Profile Building blocks for protein synthesis and cellular metabolism.
- Vitamins & Minerals
- Essential Complex Cofactors and nutrients that support enzymatic processes and overall cellular health and vitality.
Ingredient Composition Infographic
Licensed Indication
The Korean licence lists one indication: improvement of liver function in chronic liver disease. KSTATION does not describe other uses.
Therapeutic Applications
The only indication on the Korean licence is the improvement of liver function in chronic liver disease. Use is determined by the treating physician.
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
Administration Methods
• Subcutaneous injection
• Intramuscular injection
• Intramuscular injection
Recommended Injection Points for Professional Use
Product Specifications
| Specification | Value | Details |
|---|---|---|
| Package Contents | 10 / 50 Vials | 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 Ampoule or Vial | Transitioning to vials; either may ship |
| Administration Route | Injectable | SC or IM (per Korean licence) |
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
Licensed indication: Adults with chronic liver disease, for the improvement of liver function.
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
Treatment Outcomes
Outcomes are assessed by the treating physician against the licensed indication. KSTATION does not state treatment timelines or results.
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 present in the hydrolysate.
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
Going by its Korean licence, LAENNEC is given by subcutaneous or intramuscular injection. The licence does not list intravenous or intradermal use.
Dose and frequency follow the licence and the treating physician. KSTATION does not give dosing guidance.
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
Any combination with other treatments is a decision for the treating physician.
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.
JBP PLAMON Inj (2mL × 10 Amps)
6100
$61.00
Unit price perJBP PLAMON Inj (2mL × 10 Amps)
6100
$61.00
Unit price per
SUBCUTANEOUS INJECTION • PLACENTA EXTRACT
JBP PLAMON Injection
2mL x 10 Ampoules
Human placenta extract injection. MFDS-approved indication: improvement of menopausal disorder symptoms
Why KSTATION
TRUST
[MAIN PRODUCT PHOTOGRAPHY - JBP PLAMON PACKAGING AND AMPOULES]
Ingredients & Composition
ING-001
- Human Placenta Extract
- Human placenta extract, 50 mg of water-soluble substances per mL (100 mg per 2mL ampoule), as listed in the Korean MFDS product record. Contains benzyl alcohol.
High Potency Medical Grade
Approved Indication
In the Korean MFDS product record (item code 200708605), the approved indication is improvement of menopausal disorder symptoms.
MFDS
Key Facts
- Approved indication: improvement of menopausal disorder symptoms
- Human placenta extract, 50 mg water-soluble substances per mL
- For subcutaneous injection only
- Labeled course: 2mL, three times a week for two weeks
[BEFORE/AFTER RESULTS AND CLINICAL EFFECTS DOCUMENTATION]
Effects & Benefits
EFF-002
Menopausal Support
Improvement of menopausal disorder symptoms, the indication listed in the Korean MFDS product record.
Approved Indication
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 by subcutaneous injection only. Avoid nerve pathways when choosing the injection site.
3
Treatment Cycle
Typically, one ampoule (2ml) is administered three times a week for two weeks (total of six injections).
4
Site Rotation
Change the injection site each time (for example, alternate left and right) and avoid repeated injection into the same site.
[STEP-BY-STEP INJECTION TECHNIQUE AND SITE ROTATION GUIDE]
Target Recommendations
TRG-004
| Target Group | Symptoms/Condition | Benefits |
|---|---|---|
| Adults with Menopausal Symptoms | Menopausal disorder symptoms | Approved indication: improvement of menopausal disorder symptoms |
Important Safety Information
Professional administration recommended for optimal safety and effectiveness. Important precautions to ensure safe usage:
- Do not use in patients with hypersensitivity to this or other drugs
- Do not use in patients with suspected organic disease
- Do not use in patients with severe complications of the heart, liver, kidney, or other organs
- Do not use in patients with psychogenic disorders
- Do not use in newborns or premature infants (contains benzyl alcohol)
- Use with caution in patients with an allergic constitution
- Made from human placenta: donor screening and inactivation steps are applied, but the risk of infection transmission cannot be completely excluded
- 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 (50 mg/mL as water-soluble substances)
- Administration Route
- Subcutaneous injection only
- 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 injection. Its approved indication in the Korean MFDS product record is improvement of menopausal disorder symptoms.
- What is JBP PLAMON's active ingredient?
- The active ingredient is Human Placenta Extract, 50 mg of water-soluble substances per mL (100 mg per 2mL ampoule). Each box contains 10 ampoules of 2mL each.
- How is JBP PLAMON administered?
- It is administered by subcutaneous injection only. The labeled course is one 2mL ampoule three times a week for two weeks (six injections total), changing the injection site each time.
- Who should administer JBP PLAMON and what are the precautions?
- Professional administration is recommended. It must not be used in patients with hypersensitivity to this or other drugs, suspected organic disease, severe complications of the heart, liver, kidney, or other organs, or psychogenic disorders, or in newborns and premature infants (it contains benzyl alcohol). Because it is made from human placenta, the risk of infection transmission cannot be completely excluded. Sterile technique must be maintained and glass ampoules handled carefully to prevent glass fragment contamination.
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.
Cartin Inj (5mL × 10 Amps)
3000
$30.00
Unit price perCartin Inj (5mL × 10 Amps)
3000
$30.00
Unit price per
Injectable Medicine Myungmoon Pharm Prescription Only
Metabolic Support & Energy Production
Cartin Injection
(5mL x 10 Ampoules)
L-Carnitine solution for injection supporting fatty acid metabolism and energy production in patients with carnitine deficiency
#LCarnitine #MetabolicSupport #FatigueRecovery #EnergyProduction
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Active Ingredient & Mechanism of Action
Cartin injection contains L-Carnitine, a naturally occurring substance essential for mammalian energy metabolism and cellular energy production.
L-Carnitine
Primary active ingredient facilitating fatty acid transport into mitochondria
1g per 5mL ampouleHow L-Carnitine Works
L-Carnitine acts as a carrier molecule, facilitating the transport of long-chain fatty acids into the mitochondria for oxidation and subsequent energy production. This process helps the body utilize fat for energy and supports normal metabolic functions.
Mechanism
Fatty acid transport into mitochondria for energy production
Target System
Cellular energy metabolism and lipid utilization
Formulation
Injectable solution for intravenous administration
💡 Clinical Applications & Expected Effects
Metabolic Function Support
Assists in restoring normal fatty acid metabolism in deficient patients
Energy Production Enhancement
Facilitates cellular energy production through improved mitochondrial function
Fatigue Recovery
Supports recovery from fatigue related to carnitine deficiency
Carnitine Deficiency Treatment
Addresses primary and secondary carnitine deficiencies
Primary Deficiency Secondary Deficiency Hemodialysis Support Metabolic Disorders
Clinical Benefits
- Improved metabolic function in patients with carnitine deficiency
- Enhanced energy production through fatty acid oxidation
- Support for muscle activity and reduced fatigue symptoms
- Treatment of myocardial metabolic disorders
- Metabolic support for hemodialysis patients
🧪 Administration Guide & Protocol
1
Medical Assessment
Healthcare professional determines appropriate dosage based on patient condition and carnitine deficiency level
Healthcare professional determines appropriate dosage based on patient condition and carnitine deficiency level
2
Preparation
Carefully cut ampoule to minimize risk of glass fragments. Inspect solution for clarity before administration
Carefully cut ampoule to minimize risk of glass fragments. Inspect solution for clarity before administration
3
Administration Method
Administer via slow intravenous injection or intravenous drip infusion as prescribed
Administer via slow intravenous injection or intravenous drip infusion as prescribed
4
Monitoring
Monitor patient response and adjust frequency based on clinical condition and professional recommendation
Monitor patient response and adjust frequency based on clinical condition and professional recommendation
5
Disposal
Discard any unused portion immediately. Do not store opened ampoules for future use
Discard any unused portion immediately. Do not store opened ampoules for future use
Professional Administration Required
This is a prescription medication that must be administered by qualified medical professionals in clinical settings. Dosage and frequency depend on individual patient condition and doctor's recommendation.
📊 Clinical Indications & Suitable Patients
Primary Indications
Primary Carnitine Deficiency
Patients with genetic disorders affecting carnitine synthesis or transport
Secondary Carnitine Deficiency
Deficiency due to medications, diet, or medical conditions
Hemodialysis Patients
End-stage renal disease patients undergoing regular dialysis treatment
Inborn Errors of Metabolism
Patients with inherited metabolic disorders affecting fatty acid oxidation
Treatment Schedule Examples
Hemodialysis
Typically administered at the end of each dialysis session
Primary Deficiency
Dosage and frequency determined by severity and patient response
Myocardial Support
As prescribed for metabolic support of cardiac function
⚠️ Safety Information & Precautions
This prescription medication requires professional medical supervision. Follow all safety guidelines for injectable medications and proper storage procedures.
- Must be administered by qualified healthcare professionals only
- Store in sealed container at room temperature (1-30°C)
- Do not use if allergic to L-Carnitine
- Carefully handle glass ampoules to prevent contamination
Contraindications and Restrictions
- Do not use in patients with known hypersensitivity to L-Carnitine
- Exercise caution when cutting glass ampoules to prevent glass fragments
- Not for self-administration - professional medical setting required
- Discard immediately after use - do not store opened ampoules
Storage and Handling Guidelines
- Store at room temperature (1-30°C) in original packaging
- Protect from light and keep container sealed when not in use
- Check expiration date before each use - do not use expired product
- Follow institutional protocols for disposal of pharmaceutical waste
📋 Product Specifications
5mL Per Ampoule
10 Ampoules per Pack
1g L-Carnitine Content
Active Ingredient
L-Carnitine 1g per 5mL ampoule
Formulation
Clear solution for injection
Administration Route
Intravenous injection or drip infusion
Package Format
Glass ampoules (5mL x 10 units)
Storage Conditions
Room temperature (1-30°C), sealed container
Prescription Status
Prescription Only Medicine (POM)
❓ Professional Information & FAQ
A. Cartin injection is used for metabolic function support, energy production enhancement, fatigue recovery, and the treatment of primary and secondary carnitine deficiency, including support for hemodialysis patients and myocardial metabolic disorders. A. The active ingredient is L-Carnitine, 1g per 5mL ampoule, a naturally occurring substance that facilitates the transport of long-chain fatty acids into mitochondria for energy production. A. Cartin injection is administered by a qualified medical professional via slow intravenous injection or intravenous drip infusion. Dosage and frequency are determined based on the patient's condition and carnitine deficiency level. A. Cartin injection is a prescription medication that must be administered by qualified medical professionals in clinical settings. Do not use in patients with known hypersensitivity to L-Carnitine, and discard any unused portion immediately after use. A. Cartin injection is manufactured by Myungmoon Pharm. A. L-Carnitine facilitates the transport of long-chain fatty acids into mitochondria where they undergo β-oxidation for energy production. This is essential for cellular energy metabolism, particularly in muscle and cardiac tissue. A. Patients with primary or secondary carnitine deficiency, including those with inborn errors of metabolism, end-stage renal disease on
Q. What is Cartin injection used for?
Q. What is Cartin injection's active ingredient?
Q. How is Cartin injection administered?
Q. Who should administer Cartin injection and what are the precautions?
Q. Who is the manufacturer of Cartin injection?
Q. What is the mechanism of action of L-Carnitine in Cartin injection?
Q. Which patients are candidates for Cartin injection therapy?
MultiVita Inj (4ml × 10 Vials)
7200
$72.00
Unit price perMultiVita Inj (4ml × 10 Vials)
7200
$72.00
Unit price per
Multi-Vitamin Injection DAEHAN NEW Pharm Injectable Solution
Professional Vitamin Support Therapy
MultiVita Injection
4ml × 10 Vials - Complete Multi-Vitamin Complex
Comprehensive blend of essential vitamins for intravenous administration and metabolic support
#VitaminDeficiency #IVTherapy #Antioxidant #FatigueRecovery
Product packaging and vial arrangement
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧬 Key Ingredients and Formulation
Each 4ml vial contains a comprehensive blend of water-soluble and fat-soluble vitamins essential for metabolic processes and cellular function.
Ascorbic acid (Vitamin C)
Powerful antioxidant supporting immune function and collagen synthesis
Essential Vitamin
B-Complex Vitamins (B1, B2, B3, B5, B6, B7, B9, B12)
Critical co-enzymes for energy metabolism and nervous system function
Energy Support
Fat-Soluble Vitamins (A, D2, E)
Support vision health, bone metabolism, and cellular protection
Multi-FunctionVitamin molecular structure and interaction diagram
Mechanism of Action
The comprehensive blend of vitamins acts as co-enzymes in various metabolic processes, supporting energy production, cellular metabolism, and tissue repair. Antioxidant vitamins C and E help neutralize free radicals, protecting cells from oxidative stress and supporting overall health.
Primary Function
Co-enzyme support for metabolic processes
Antioxidant Action
Free radical neutralization and cell protection
Delivery System
Intravenous administration for direct bioavailability
💡 Expected Effects and Benefits
Vitamin Deficiency Prevention
Comprehensive vitamin replacement therapy for deficiency states
General Vitality Support
Enhanced energy levels and reduced fatigue symptoms
Metabolic Function Enhancement
Improved cellular metabolism and energy production pathways
Antioxidant Protection
Cellular protection from oxidative stress and free radical damage
Energy Production Immune Support Antioxidant Cellular Function
Primary Benefits
- Prevention and treatment of vitamin deficiency conditions
- Support for patients with increased nutritional requirements
- Enhanced recovery during illness, surgery, or trauma
- Maintenance therapy for patients receiving fluid nutrition
Clinical benefits visualization chart
Designed for comprehensive vitamin maintenance therapy in clinical settings where nutritional needs are supplied via fluid administration.
🧪 Administration Protocol
1
Pre-Administration Check
Verify solution clarity and absence of particulate matter. Check expiration date and patient allergy history.
Verify solution clarity and absence of particulate matter. Check expiration date and patient allergy history.
2
Dilution Preparation
Mix single 4ml dose with 500-1000ml of standard IV fluid (dextrose or saline solution).
Mix single 4ml dose with 500-1000ml of standard IV fluid (dextrose or saline solution).
3
Light Protection
Minimize exposure to light during preparation due to light-sensitive vitamins (A, D, Riboflavin).
Minimize exposure to light during preparation due to light-sensitive vitamins (A, D, Riboflavin).
4
IV Administration
Administer via intravenous infusion over appropriate time period as prescribed.
Administer via intravenous infusion over appropriate time period as prescribed.
5
Post-Administration
Use diluted solution within 24 hours. Dispose of any unused portion properly.
Use diluted solution within 24 hours. Dispose of any unused portion properly.
Typically administered once daily as prescribed by healthcare professional. Professional administration required.
IV administration technique and dilution guide
📊 Product Specifications
4ml Per Vial
10 Vials per Box
IV Administration Route
Formulation
Liquid solution for injection
Administration
Intravenous infusion after dilution
Packaging
4ml glass vials, 10 vials per carton
Professional Use
Healthcare professional administration required
⚠️ Safety Information and Precautions
Professional Use Only: This product must be administered by qualified healthcare professionals only. Do not administer undiluted.
- Professional medical supervision required during administration
- Proper dilution with standard IV fluids is mandatory
- Use diluted solution within 24 hours of preparation
- Minimize light exposure during handling and administration
Contraindications and Warnings
- Do not use if solution is cloudy or contains particulate matter
- Discontinue if any adverse reactions occur during infusion
- Not for direct injection - must be diluted before administration
- Dispose of unused portion after 24 hours of dilution
Storage and Handling
- Store below 25°C in light-resistant container
- Keep away from direct sunlight and heat sources
- Keep container tightly closed when not in use
- Check expiration date before each use
❓ Frequently Asked Questions
A. MultiVita Injection is used for vitamin deficiency prevention, general vitality support, metabolic function enhancement, antioxidant protection, and nutritional support during illness, surgery, or trauma. A. Each 4ml vial contains a comprehensive multi-vitamin complex: Ascorbic acid (Vitamin C), B-Complex Vitamins (B1, B2, B3, B5, B6, B7, B9, B12), and fat-soluble Vitamins A, D2, and E. A. A single 4ml dose must be diluted with 500-1000ml of standard IV fluid (dextrose or saline) and administered via intravenous infusion by a healthcare professional, typically once daily. It must never be injected undiluted. A. Only qualified healthcare professionals should administer this product under medical supervision. Do not use if the solution is cloudy or contains particulate matter, discontinue if adverse reactions occur, and use diluted solution within 24 hours. A. MultiVita Injection is manufactured by DAEHAN NEW Pharm. A. No, this product must be properly diluted with 500-1000ml of standard IV fluid before administration. Direct injection is contraindicated. A. The diluted solution should be used within 24 hours of preparation and stored away from direct light due to light-sensitive vitamins. A. It's used for vitamin deficiency prevention, nutritional support during illness, surgery, trauma, and maintenance therapy for patients receiving fluid nutrition. A. Store below 25°C in a light-resistant container, away from direct sunlight. Keep tightly closed and check expiration dates regularly.
Q. What is MultiVita Injection used for?
Q. What is MultiVita Injection's active ingredient?
Q. How is MultiVita Injection administered?
Q. Who should administer MultiVita Injection and what are the precautions?
Q. Who is the manufacturer of MultiVita Injection?
Q. Can this be injected directly without dilution?
Q. How should the diluted solution be stored?
Q. What conditions is this product used for?
Q. Are there any storage requirements?
HYCOMIN Inj (2mL × 50 Amps)
7800
$78.00
Unit price perHYCOMIN Inj (2mL × 50 Amps)
7800
$78.00
Unit price perVitamin B12 Injection
HYCOMIN
2mL x 50 Ampoules
Professional Hydroxocobalamin B12 Injection for Fatigue Recovery & Metabolic Support
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
🧩 Essential Product Information
Premium Vitamin B12 Injection Solution
HYCOMIN injection contains high-grade Hydroxocobalamin, a bioactive form of Vitamin B12 that serves as a vital coenzyme for various metabolic functions. This professional-grade solution supports fat and carbohydrate metabolism, protein synthesis, cell replication, and nervous system maintenance for optimal health and energy recovery.
Active Ingredient
Hydroxocobalamin
2.5mg/mL
Bioactive Vitamin B12 form for enhanced absorption
Formulation
Injectable
Solution
Package Size
2mL
per ampoule
Quantity
50
Ampoules
2.5mg High-Potency B12
📋 Detailed Product Specifications
| Specification | Details | Benefits |
|---|---|---|
| Active Ingredient | Hydroxocobalamin 2.5mg/mL | Bioactive form of Vitamin B12 |
| Formulation Type | Injectable Solution | Direct absorption, maximum bioavailability |
| Administration | Intramuscular/Intravenous | Professional medical application |
| Storage Requirements | 1-30°C, away from light | Maintains potency and stability |
| Package Contents | 50 x 2mL Ampoules | Convenient professional supply |
| Application Method | Single-use injection | Sterile, contamination-free |
🧬 Mechanism of Action & Benefits
💡 Clinical Benefits & Effects
Primary Health Benefits
HYCOMIN injection provides comprehensive support for individuals with Vitamin B12 deficiency, offering rapid restoration of depleted B12 stores and supporting overall metabolic health and energy levels.
Fatigue Recovery
Metabolic Support
Nervous System Health
Therapeutic Applications
Specifically designed for the prevention and treatment of Vitamin B12 deficiency in patients requiring rapid correction of B12 levels.
- Treatment of confirmed Vitamin B12 deficiency
- Support for chronic fatigue related to B12 deficiency
- Maintenance of nervous system health
- Enhancement of overall metabolic function
🧪 Professional Usage Protocol
1
Medical Assessment
Patient evaluation and B12 deficiency confirmation by qualified healthcare professional. Dosage and frequency determined based on individual condition severity.
2
Preparation & Administration
Professional preparation of injection site and sterile administration via intramuscular or intravenous injection by qualified medical personnel.
3
Treatment Schedule
Initial treatment may involve daily injections, followed by weekly or monthly maintenance schedule as determined by healthcare provider based on patient response.
4
Monitoring & Follow-up
Regular monitoring of blood B12 levels and patient response. Adjustment of treatment frequency based on clinical assessment and laboratory results.
📊 Treatment Comparison
| Purpose | Key Ingredients | Administration | Primary Benefits |
|---|---|---|---|
| Vitamin B12 Deficiency | Hydroxocobalamin | Intramuscular/Intravenous | Corrects B12 deficiency, supports metabolism |
| Skin Enhancement | Glutathione, Vitamin C | Intravenous | Antioxidant, skin brightening |
| Liver Support | Placental Extract | Intramuscular | Liver function, anti-inflammatory |
Important Safety Information
This is a prescription medication that must be administered by qualified medical professionals. Proper safety protocols and patient assessment are essential for safe and effective use.
- Do not use in patients with known hypersensitivity to Hydroxocobalamin or cobalt
- Store in cool, dry place away from light at 1-30°C temperature range
- Single-use only - discard any unused portion to prevent contamination
- Monitor for potential side effects including injection site pain or allergic reactions
- Professional medical supervision required for administration and monitoring
❓ Frequently Asked Questions
What is HYCOMIN used for?
HYCOMIN is used for the prevention and treatment of Vitamin B12 deficiency, support for chronic fatigue related to B12 deficiency, maintenance of nervous system health, and enhancement of overall metabolic function.
What is HYCOMIN's active ingredient?
The active ingredient is Hydroxocobalamin, 2.5mg/mL, a bioactive form of Vitamin B12 that serves as a vital coenzyme for metabolic functions.
How is HYCOMIN administered?
HYCOMIN is administered by qualified medical personnel via intramuscular or intravenous injection. Initial treatment may involve daily injections, followed by a weekly or monthly maintenance schedule based on patient response.
Who should administer HYCOMIN and what are the precautions?
HYCOMIN is a prescription medication that must be administered by qualified medical professionals under supervision. Do not use in patients with known hypersensitivity to Hydroxocobalamin or cobalt. It is single-use only - discard any unused portion.
Treatment Duration
Variable
Per Condition
Application Setting
Professional
Medical Only
Manufacturing
Pharmaceutical
Grade
Quality Standard
Medical
Approved
BC ASCORBIC Inj (20mL × 10 Vials)
4000
$40.00
Unit price perBC ASCORBIC Inj (20mL × 10 Vials)
4000
$40.00
Unit price per
Injectable Vitamin • Ascorbic Acid
BC ASCORBIC Injection
Vitamin C • 20mL x 10 Vials
Ascorbic acid injection for acute cases or when oral administration is difficult, per its MFDS-listed indications
Why KSTATION
KST-000
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Composition & Formulation
COMP-001
- Ascorbic Acid (Vitamin C)
- Active ingredient, KP grade. Each 20mL vial contains 10g of ascorbic acid (500mg/mL concentration).
500mg/mL Pharmaceutical Grade
- Sterile Water for Injection
- Water for injection, listed as an inactive ingredient in the MFDS record together with sodium hydroxide, sodium bicarbonate, and edetate sodium hydrate.
Excipient
Effects & Benefits
EFF-002
10g
Per Vial Content
500mg/mL
Concentration
20mL
Volume Per Vial
MFDS-Listed Indications
For acute cases or when oral administration is difficult:
- Prevention and treatment of vitamin C deficiency, such as scurvy
- Increased vitamin C requirement, such as pregnancy, lactation, or heavy physical labor
- Capillary bleeding (nosebleed, gum bleeding, hematuria) presumed to involve vitamin C deficiency or metabolic disorder
- Bone matrix formation and promotion of fracture healing
- Melasma, freckles, and post-inflammatory pigmentation; photosensitive dermatitis
Usage & Administration
ADM-003
1
Preparation
Injection is used in acute cases or when oral administration is difficult. Switch to oral administration once it is possible and sufficient. Use sterile technique.
2
Administration
Ascorbic acid 50 to 1,000 mg per day, once daily or in divided doses, by subcutaneous, intramuscular, or intravenous injection. Adjust according to age and symptoms.
3
Monitoring
Inject intravenously as slowly as possible; rapid injection may cause transient fainting, dizziness, or vascular pain. For subcutaneous or intramuscular use, avoid nerve pathways and do not inject repeatedly into the same site.
Product Specifications
SPEC-004
| Specification | Value | Standard |
|---|---|---|
| Active Ingredient | Ascorbic Acid | KP (Korean Pharmacopoeia) |
| Concentration | 500mg/mL | Pharmaceutical Grade |
| Volume per Vial | 20mL | |
| Total Vials | 10 Vials | Package Unit |
Storage & Handling Conditions
- Temperature: Store at 2°C to 8°C (36°F to 46°F), in a sealed light-resistant container
- Light Protection: Store in original amber vials to protect from light
- Humidity: Keep in dry conditions, avoid moisture exposure
- Shelf Life: 24 months from manufacture date when stored properly
Important Safety Information
Professional medical supervision required for administration.
- Do not use in hypersensitivity to its ingredients, hyperoxaluria, thalassemia, gout, or cystinuria
- Do not use in G6PD deficiency (high doses may cause hemolysis)
- Do not use at 1 g or more per day in patients with oxalate kidney stones
- May interfere with urine glucose and occult blood tests
- Consult healthcare provider if pregnant or breastfeeding
Clinical Applications
CLIN-005
Pigmentation
Listed in the MFDS record among conditions presumed to involve vitamin C deficiency or metabolic disorder: melasma, freckles, and post-inflammatory pigmentation; photosensitive dermatitis.
MFDS Indication
Quality Assurance
QA-006
🏆
KP Grade
Korean Pharmacopoeia (KP) specification
✅
GMP Certified
Good Manufacturing Practice compliance
🔬
Sterility Tested
Rigorous sterility and purity testing
🛡️
MFDS Registered
Korea Ministry of Food and Drug Safety, item code 200909290
Administration Protocols
PROT-A
Labeled Dosing (MFDS)
Ascorbic acid 50 to 1,000 mg per day, once daily or in divided doses, adjusted according to age and symptoms.
Routes: SC / IM / IV
Daily Dose: 50 to 1,000 mg
IV Rate: As slowly as possible
Technical Documentation
TECH-008
Package Information
- Package Type
- Vial, 20mL each, 10 vials per box
- Vial Material
- Amber glass vials with rubber stopper and aluminum seal
- Volume
- 20mL per vial, 10 vials per package (200mL total)
- Concentration
- 500mg/mL (50% w/v) ascorbic acid solution
- Batch Tracking
- Complete lot number traceability for quality assurance
Professional Guidelines
- Must be used in professional clinical settings only
- Requires proper medical supervision during administration
- Complete sterile technique must be maintained
Frequently Asked Questions
FAQ-009
What is BC ASCORBIC Injection used for?
BC ASCORBIC Injection is used in acute cases or when oral administration is difficult, for the indications in its Korean MFDS record: prevention and treatment of vitamin C deficiency such as scurvy; increased vitamin C requirement such as pregnancy, lactation, or heavy physical labor; and conditions presumed to involve vitamin C deficiency or metabolic disorder, including capillary bleeding, bone matrix formation and fracture healing, melasma, freckles, post-inflammatory pigmentation, and photosensitive dermatitis.
What is BC ASCORBIC Injection's active ingredient?
The active ingredient is Ascorbic Acid (Vitamin C) at a concentration of 500mg/mL, with each 20mL vial containing 10g of ascorbic acid.
How is BC ASCORBIC Injection administered?
The labeled dose is ascorbic acid 50 to 1,000 mg per day, given once daily or in divided doses by subcutaneous, intramuscular, or intravenous injection, adjusted for age and symptoms. Intravenous injection should be given as slowly as possible.
Who should administer BC ASCORBIC Injection and what are the precautions?
It requires professional medical supervision. It must not be used in patients with hypersensitivity to its ingredients, hyperoxaluria, thalassemia, gout, cystinuria, or G6PD deficiency, or at 1 g or more per day in patients with oxalate kidney stones. It may interfere with urine glucose and occult blood tests, and pregnant or breastfeeding patients should consult a healthcare provider.
This professional-grade ascorbic acid injection meets the highest pharmaceutical standards for quality, purity, and efficacy. Manufactured under strict GMP conditions with comprehensive quality control testing to ensure consistent therapeutic outcomes and patient safety.
KP Grade
GMP Certified
MFDS Registered
Ginkgo Inj (5mL × 25 Amps)
4000
$40.00
Unit price perGinkgo Inj (5mL × 25 Amps)
4000
$40.00
Unit price perGinkgo Injection Product Image
Ginkgo Injection
5mL x 25 Ampoules
Professional Injectable Solution
Advanced Ginkgo Biloba extract injection for enhanced cerebral and peripheral circulation, cognitive support, and vascular health improvement.
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Product Overview
Ginkgo Injection Product Image
Professional Use Only
Premium Ginkgo Biloba Extract
Each ampoule contains 17.5mg of high-quality dried Ginkgo Biloba leaf extract in a sterile 5mL solution. Formulated for professional medical administration to support circulation and cognitive function.
- Enhanced cerebral and peripheral blood circulation
- Antioxidant and anti-inflammatory properties
- Cognitive function and memory support
- Relief for dizziness and tinnitus
Active Ingredients & Mechanism
- Ginkgo Biloba Leaf Extract
- 17.5mg per 5mL Contains active compounds including ginkgo flavone glycosides and terpene trilactones with multifaceted therapeutic effects.
- Ginkgo Flavone Glycosides
- Antioxidant Primary bioactive compounds that provide potent antioxidant properties and help neutralize free radicals.
- Terpene Trilactones
- Vasoactive Essential components that promote vasodilation and improve blood vessel function.
Ginkgo Biloba Mechanism of Action Infographic
Multi-Modal Action
The extract works through multiple pathways: improving blood circulation, reducing oxidative stress, protecting against cellular damage, and enhancing oxygen and nutrient delivery to tissues.
Clinical Benefits
Cerebral
Circulation Support
Peripheral
Vascular Health
Cognitive
Function Enhancement
Memory
Improvement
- Alleviates symptoms of cerebrovascular insufficiency
- Improves blood flow to extremities
- Reduces symptoms of intermittent claudication
- Provides neuroprotective effects
Long-term Vascular Health
Regular administration supports overall vascular health by protecting blood vessels from oxidative damage and maintaining optimal circulation throughout the body.
Administration Protocols
Standard Treatment Protocol
Daily intramuscular or intravenous injection of 5-10mL, or intravenous injection of 15mL every two days as determined by healthcare professional.
Acute Treatment Protocol
For acute conditions: 25mL daily by intravenous drip. For severe cases: 25-50mL daily by intravenous injection or IV drip.
Injection Site Guide and Administration Technique
Professional Administration Required
This product requires administration by qualified medical professionals in clinical settings. Each ampoule is designed for single use to ensure sterility and precise dosing.
Treatment Applications
| Treatment Strategy | Key Benefits | Administration Method | Precautions |
|---|---|---|---|
| Cerebrovascular Support | Improved cerebral blood flow, cognitive enhancement, memory support | IV/IM injection | Avoid with anticoagulants |
| Peripheral Vascular Support | Enhanced circulation to extremities, claudication relief | IV/IM injection | Monitor with blood thinners |
Safety Information & Storage
Important Safety Information
Professional use only. This product requires careful handling and administration by qualified healthcare providers.
- Not for use in pregnant or breastfeeding women
- Contraindicated with bleeding disorders
- Avoid concurrent use with anticoagulants
- Single-use ampoules - discard after opening
- Do not consume raw ginkgo seeds
Storage Requirements
Store in sealed container, protected from light, at room temperature (1-30°C). Each ampoule is intended for single use and any remaining solution should be discarded after opening.
Contraindications
Do not use in patients with known hypersensitivity to ingredients, bleeding disorders, or increased bleeding risk. Use with caution in patients taking anticoagulant or antiplatelet medications.
Product Specifications
25
Ampoules per Box
5mL
Volume per Ampoule
17.5mg
Extract per Ampoule
Package Specifications and Product Details
Quality Assurance
Manufactured to pharmaceutical standards with rigorous quality control. Each batch is tested for purity, potency, and sterility to ensure consistent therapeutic efficacy.
Frequently Asked Questions
What is Ginkgo Injection used for?
Ginkgo Injection is used for enhanced cerebral and peripheral blood circulation, cognitive function and memory support, relief for dizziness and tinnitus, alleviation of cerebrovascular insufficiency, and relief of intermittent claudication symptoms.
What is Ginkgo Injection's active ingredient?
The active ingredient is dried Ginkgo Biloba leaf extract, 17.5mg per 5mL ampoule, containing ginkgo flavone glycosides (antioxidant) and terpene trilactones (vasoactive).
How is Ginkgo Injection administered?
Ginkgo Injection is administered by a healthcare professional via intramuscular or intravenous injection. The standard protocol is 5-10mL daily, or 15mL every two days by IV; for acute conditions, 25mL daily by IV drip, and for severe cases 25-50mL daily.
Who should administer Ginkgo Injection and what are the precautions?
Ginkgo Injection must be administered by qualified medical professionals in clinical settings. It is not for use in pregnant or breastfeeding women, is contraindicated with bleeding disorders, and should not be used concurrently with anticoagulants or antiplatelet medications.
Juveheal A (5mL × 5 Vials)
5800
$58.00
Unit price perJuveheal A (5mL × 5 Vials)
5800
$58.00
Unit price per
Product Identification
Juveheal A Ampoule
Anti-Aging & Wrinkle Care
J MEDICAL Inter Co., Ltd. Sterile Ampoule
Total Volume/Content
5mL × 5 Vials
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
Adenosine 0.04%, EGF (Rh-Oligopeptide-1), FGF2 (Rh-Polypeptide-1), Hydrolyzed Collagen
Key Secondary Ingredients
Lotus Flower Water (Nelumbo Nucifera), Beta-Glucan, Allantoin, Centella Asiatica Extract
Mechanism of Action
Juveheal A features a dual growth factor action where EGF repairs the epidermis and FGF2 stimulates the dermis for improved skin density. Adenosine actively encourages collagen production to correct fine lines, while the Lotus water base provides deep hydration and soothing effects.
Dual Growth Factors Adenosine Anti-Wrinkle Lotus Water Base
Efficacy Summary & Expected Benefits
Main Effects and Benefits
- Anti-Aging & Wrinkle Improvement: Specifically targets fine lines and deep wrinkles.
- Skin Vitality & Radiance: Restores a healthy glow to tired or aging skin.
- Elasticity Boost: Improves skin firmness and lifting effect.
- Deep Nutrition: Delivers concentrated nutrients to the skin layers.
Recommended/Targeted Areas
Full face (especially areas with fine lines like eyes, forehead, nasolabial folds), Neck.
Usage Protocol & Application Guide
Recommended Application Method
Topical application after cleansing. Highly recommended for use with professional devices like MTS, Derma Pen, or Electroporation to enhance absorption.
Treatment Cycle/Frequency
Typically 1 session per week (standard MTS protocol).
Preparation Instructions
Ready-to-use liquid ampoule (tear off the plastic cap and aluminum seal to open).
Juveheal Series Comparison
| Product | Label Color | Primary Indication |
|---|---|---|
| Juveheal A | Brown/Gold | Anti-Aging, Wrinkle Care (Adenosine + EGF) |
| Juveheal B | Blue | Lifting, Pore Reduction (Peptide + PDRN) |
| Juveheal W | White/Silver | Whitening, Tone Up (Niacinamide) |
Select "Juveheal A" specifically for patients concerned with aging signs, loss of elasticity, and wrinkles.
Storage & Handling Instructions
Required Storage Temperature
Room temperature (1–30°C). Keep cool.
Shelf Life
Typically 3 years from manufacturing date. Use immediately after opening.
General Handling
Avoid direct sunlight, high temperature, and high humidity.
Precautions & Safety Notes
Contraindications Do not apply to open wounds or areas with eczema/dermatitis. Known allergy to any ingredients (e.g., Lotus flower).
Safety Warnings For external use only (Topical). Avoid contact with eyes.
Common Temporary Side Effects
- Mild redness or irritation may occur, especially if used with MTS/microneedling (subsides within 1-2 days).
Post-Treatment Care
- Use a soothing mask (e.g., cooling sheet mask) after application.
- Apply sun protection.
Frequently Asked Questions
What is Juveheal A used for?
Juveheal A is an anti-aging and wrinkle care ampoule. It targets fine lines and deep wrinkles, restores skin vitality and radiance, boosts elasticity and firmness, and delivers deep nutrition to the skin.
What are the key ingredients?
The primary active ingredients are Adenosine 0.04%, EGF (Rh-Oligopeptide-1), FGF2 (Rh-Polypeptide-1), and Hydrolyzed Collagen, with a Lotus Flower Water base.
How is it applied?
It is a ready-to-use liquid ampoule applied topically after cleansing. It is highly recommended for use with professional devices such as MTS, Derma Pen, or Electroporation to enhance absorption, typically 1 session per week.
Who should administer Juveheal A?
Juveheal A is for external (topical) use only. For enhanced absorption it is used with professional devices such as MTS, Derma Pen, or Electroporation under professional guidance.
Who manufactures Juveheal A?
Juveheal A is manufactured by J MEDICAL Inter Co., Ltd.
Keywords & Search Terms
Juveheal A Anti-aging Ampoule EGF Ampoule Adenosine Wrinkle Care MTS Serum Skin Booster Growth Factors
Lipotocin Inj (12mL x 10 Amps)
4100
Lipotocin Inj (12mL x 10 Amps)
4100
Product Identification
Lipotocin Inj.
High Dose Cinderella Injection
South Korean Manufacturer IV Injection Ampoule
Total Volume/Content
120mL per box (12mL × 10 Ampoules)
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
Core Ingredients & Technology
Primary Active Ingredients
Thioctic Acid (Alpha-Lipoic Acid) 300mg
Mechanism of Action
Thioctic Acid acts as an antioxidant master, regenerating Vitamin C, E, and Glutathione while scavenging free radicals. It also increases mitochondrial energy expenditure to aid in lipolysis (fat breakdown) and prevents protein glycation to reduce tissue aging.
Thioctic Acid 300mg High Dose Metabolic Activation Anti-Glycation
Efficacy & Benefits
Main Effects
- Intensive Anti-Aging: Powerful antioxidant protection against cellular damage.
- Skin Brightening: Reduces dullness and improves skin texture ("Baby Face Injection").
- Body Slimming: Boosts metabolism to aid in weight loss and reduce edema.
- Fatigue Recovery: Improves energy levels and exhaustion.
- Diabetic Neuropathy Relief: Relieves sensory abnormalities.
Targeted Use
Systemic IV Drip Skin Tone Improvement Metabolic Boost
Usage Protocol
Dilution Required Do not inject undiluted directly ("IV Push") as it causes vascular pain and potential shock.
Application Method
Intravenous Drip (IV Infusion)
Dilution Protocol
Mix 1 ampoule (12mL) with 100mL – 250mL of Normal Saline.
Infusion Speed
Administer slowly over at least 15–30 minutes.
Treatment Cycle
1–2 times per week; standard course of 10 sessions.
Product Comparison
| Product Version | Thioctic Acid Content | Primary Strategy |
|---|---|---|
| Lipotocin (High Dose) | 300mg / 12mL | Intensive Slimming & Metabolic Boost |
| Standard Cindella (Low Dose) | 25mg / 5mL | Cocktail Maintenance (Mixed with Vit C/Glutathione) |
Storage & Handling
Required Storage Temperature
Room temperature (1°C – 30°C)
Light Sensitivity
Strictly Protect from Light. Keep ampoules in the original box until use.
Shelf Life
24–36 months from manufacture date
Precautions & Safety
Contraindications Do not use in children/adolescents or patients with hypersensitivity to Thioctic Acid.
Safety Warnings Rapid infusion can cause headache, nausea, and respiratory distress. Diabetics should monitor glucose levels as Thioctic acid may cause hypoglycemia.
Common Temporary Side Effects
- Nausea, vomiting, or gastrointestinal discomfort (rare with slow drip).
- Skin rash or itching at the injection site.
Post-Treatment Care
Avoid heavy alcohol consumption as it interferes with metabolic effects.
Frequently Asked Questions
What is Lipotocin Inj. used for?
Lipotocin Inj. is a high-dose Thioctic Acid (Cinderella) injection used for intensive anti-aging antioxidant protection, skin brightening, body slimming through metabolic boost and edema reduction, fatigue recovery, and relief of diabetic neuropathy (sensory abnormalities).
What is Lipotocin's active ingredient?
The primary active ingredient is Thioctic Acid (Alpha-Lipoic Acid) at 300mg per 12mL ampoule. It acts as an antioxidant master, regenerating Vitamins C and E and Glutathione, increasing mitochondrial energy expenditure to aid lipolysis, and preventing protein glycation.
How is Lipotocin administered?
Lipotocin is administered as an intravenous drip (IV infusion). One ampoule (12mL) is diluted with 100mL–250mL of normal saline and infused slowly over at least 15–30 minutes. It must not be injected undiluted as an IV push, which can cause vascular pain and potential shock. The standard cycle is 1–2 times per week for a course of 10 sessions.
Who should not use Lipotocin and what are the precautions?
Lipotocin is contraindicated in children and adolescents and in patients with hypersensitivity to Thioctic Acid. Rapid infusion can cause headache, nausea, and respiratory distress, and diabetics should monitor glucose levels as Thioctic Acid may cause hypoglycemia. Heavy alcohol consumption should be avoided as it interferes with the metabolic effects.
Keywords
Lipotocin Thioctic Acid 300mg Alpha Lipoic Acid High Dose Cindella Cinderella Injection Fat Burn Injection Antioxidant IV Metabolism Booster
MELSMON Inj (2mL × 50 Amps)
41000
$410.00
Unit price perMELSMON Inj (2mL × 50 Amps)
41000
$410.00
Unit price perProfessional Injectable
MELSMON injection
2mL x 50 Ampoules
Human placenta extract injection. MFDS-approved indication: improvement of menopausal disorder symptoms
Why KSTATION
Why KSTATION
100% Authentic
Genuine Korean supply
97% Clearance
Proven customs success rate
Cold-Chain
Temperature-controlled shipping
[MELSMON Product Package and Ampoule Photography]
Composition
Key Components
Human Placenta Extract
100mg per 2mL
Human placenta extract, 50 mg of water-soluble substances per mL (100 mg per 2mL ampoule), as listed in the Korean MFDS product record. Contains benzyl alcohol.
[Molecular Structure and Bioactive Components Infographic]
Indication
Approved Indication
1
Menopausal Symptom Improvement
Improvement of menopausal disorder symptoms, the indication listed in the Korean MFDS product record (item code 200308393).
[Before & After Results and Clinical Benefits Visualization]
Administration
Professional Usage Protocol
1
Pre-Treatment Assessment
Comprehensive patient evaluation and treatment area assessment by qualified healthcare professional to determine optimal injection protocol and dosage requirements.
2
Professional Administration
Subcutaneous injection only, using sterile technique. Avoid nerve pathways and change the injection site each time (for example, alternate left and right).
3
Treatment Schedule
2mL per dose, three times a week for two weeks (six injections in total), as labeled in the MFDS record.
4
Progress Monitoring
Regular assessment of treatment response and adjustment of protocol as needed to ensure optimal therapeutic outcomes and patient satisfaction.
[Professional Administration Technique Guide and Injection Areas]
Treatment Protocols
Recommended Applications by Target
Menopausal Support Protocol
For menopausal disorder symptoms, the approved indication in the MFDS record. Labeled course: 2mL subcutaneously, three times a week for two weeks.
[Treatment Protocol Infographic and Professional Guidelines]
| Specification | Details |
|---|---|
| Package Contents | 50 Ampoules × 2.0 mL each |
| Active Ingredient | Human Placenta Extract 100mg per ampoule |
| Administration Route | Subcutaneous Injection only |
| Storage Temperature | 1-30°C (Room Temperature) |
| Treatment Duration | 2 weeks (6 injections, 3 per week) |
| Professional Use | Qualified Healthcare Professional Required |
Important Safety Information
Professional use only. Do not use in patients with hypersensitivity to this or other drugs, suspected organic disease, severe complications of the heart, liver, kidney, or other organs, or psychogenic disorders, or in newborns and premature infants (contains benzyl alcohol). Use with caution in patients with an allergic constitution. Made from human placenta: donor screening and inactivation steps are applied, but the risk of infection transmission cannot be completely excluded. Stop use if shock, chills, nausea, fever, redness, rash, breast pain, or gynecomastia occur; pain or redness at the injection site may occur. Cut glass ampoules carefully to minimize glass fragments. Store in a sealed container at 1 to 30°C. Always administered by qualified healthcare professional.
[Product Documentation, Regulatory Compliance, and Professional Guidelines]
Frequently Asked Questions
Frequently Asked Questions
What is MELSMON injection used for?
MELSMON injection is a human placenta extract injection. Its approved indication in the Korean MFDS product record is improvement of menopausal disorder symptoms.
What is MELSMON's active ingredient?
The active ingredient is Human Placenta Extract, 50 mg of water-soluble substances per mL (100 mg per 2mL ampoule). It contains benzyl alcohol.
How is MELSMON administered?
MELSMON is administered by subcutaneous injection only, using sterile technique. The labeled course is 2mL per dose, three times a week for two weeks (six injections total), changing the injection site each time.
Who should administer MELSMON and what are the precautions?
MELSMON is for professional use only and must be administered by a qualified healthcare professional. It must not be used in patients with hypersensitivity to this or other drugs, suspected organic disease, severe complications of the heart, liver, kidney, or other organs, or psychogenic disorders, or in newborns and premature infants (it contains benzyl alcohol). Because it is made from human placenta, the risk of infection transmission cannot be completely excluded. Injection site pain or redness may occur; stop use if shock or hypersensitivity symptoms appear.
MELSMON Excellence
MELSMON injection is a human placenta extract injection imported into Korea by Korea Melsmon Co., Ltd. Its approved indication in the MFDS product record is improvement of menopausal disorder symptoms.
Rejuva Booster (3mL × 2 Vials)
3600
$36.00
Unit price perRejuva Booster (3mL × 2 Vials)
3600
$36.00
Unit price per
Product Identification
Rejuva Booster
Whitening & Hydration Skin Booster
Phace Global Co., Ltd. Glutathione Enriched Water Glow Effect
Total Volume/Content
3mL × 2 Vials (Sterile)
Formulation Type
Liquid solution (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
Cross-linked Hyaluronic Acid (10 mg/mL), Glutathione (1 mg/mL)
Mechanism of Action
Advanced Cross-linked HA creates a stable 3D matrix to lock in moisture and restore elasticity, while Glutathione acts as a powerful antioxidant to brighten skin tone, fade pigmentation, and detoxify tired skin.
Cross-linked HA Matrix Glutathione Brightening Long-lasting Hydration
Efficacy & Benefits
Main Effects
- Deep & Long-Lasting Hydration: Locks in moisture for months.
- Radiance & Tone: Brightens skin tone and fades pigmentation (Whitening effect).
- Elasticity & Plumping: Restores firmness and smooths fine lines.
- Detox & Protection: Fights oxidative stress and revitalizes congested skin.
Targeted Areas
Face (Under-eye, Cheeks, Forehead, Perioral) and Body (Neck, Hands, Knees, Elbows, Underarms/Bikini for brightening).
Usage Protocol
Standard Treatment Cycle
5 sessions total, spaced 2–3 weeks apart.
Injection Guidelines
| Method | Target Area | Depth |
|---|---|---|
| Micropapular | Under-eye, Forehead, Neck | 0.3–0.8 mm |
| Nappage | Neck, Perioral, Body | Superficial Dermis |
| Linear / Retrograde | Cheeks, Hands | 0.8–1.5 mm |
Pro Tip Inject slowly and evenly. Avoid intradermal or too superficial placement to prevent bumps, as this formula uses cross-linked HA.
Rejuva Series Comparison
| Product | Active Ingredients | Key Focus |
|---|---|---|
| Rejuva Booster | Cross-linked HA + Glutathione | Brightening (Whitening) & Long-lasting Hydration |
| Rejuva Healer S | HA + PDRN + NAD+ | Cellular Energy & Anti-aging |
| Rejuva Healer V | HA + PDRN | Intensive Regeneration |
Choose Rejuva Booster for patients specifically seeking the "Water Glow" effect combined with skin tone brightening.
Storage & Handling
Storage Conditions
1–30°C (Cool, dry place). Keep away from direct sunlight.
Shelf Life
Refer to package expiry (typically 24–36 months).
Usage Note
Single-use vials. Discard any remaining solution after opening.
Safety Information
Contraindications Hypersensitivity to HA or Glutathione; Pregnancy and breastfeeding; Active skin infections.
Safety Warnings For external/professional use only. Avoid contact with eyes or mucous membranes. Use smaller gauge needles (30–32G) for sensitive areas.
Keywords
Rejuva Booster Glutathione Injection Cross-linked HA Skin Brightening Whitening Injection Hydration Booster Korean Skin Booster
Frequently Asked Questions
What is Rejuva Booster used for?
It is a whitening and hydration skin booster that brightens skin tone, fades pigmentation, and delivers deep long-lasting hydration for the face and body.
What are the key ingredients?
Cross-linked Hyaluronic Acid (10 mg/mL) and Glutathione (1 mg/mL), combining a moisture-locking HA matrix with antioxidant brightening.
How long does the treatment cycle take?
A standard course is 5 sessions total, spaced 2–3 weeks apart.
Who should administer it?
For external/professional use only, injected by a qualified practitioner using micropapular, nappage, or linear/retrograde techniques.
Who manufactures Rejuva Booster?
It is manufactured by Phace Global Co., Ltd.