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Gluthion Inj 600mg
Gluthion Inj 600mg is a high-concentration glutathione injection originating from South Korea, containing 10 vials of sterile lyophilized powder per box (600mg/vial). Data from the Korean Institute of Dermatological Sciences demonstrates its ability to reduce melanin production by 38%-52% through tyrosine enzyme activity inhibition, effectively addressing hyperpigmentation (melasma, acne scars) and brightening skin tone.
$49.00
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 4% | $47.04 |
| 10-19 | 8% | $45.08 |
| 20-Unlimited | 10% | $44.10 |
Gluthion Inj 600mg | Medical-Grade Formulation
Glutathione injection 600mg(HPLC purity ≥99.2%) with dual-action antioxidant therapy. Clinical data from the Korean pharmaceutical company demonstrated that reduce melasma area by 45.3% (MASI score) in 8 weeks and elevate hepatic detoxification enzymes by 27%. Achieves peak serum concentration of 12.5μg/mL within 1 hour (92% bioavailability).With 94% free radical scavenging rate, this formulation enhances hepatic detoxification, supports ocular health, and boosts immune function. The freeze-dried preparation ensures optimal stability and bioavailability for clinical-grade antioxidant therapy.
Key Therapeutic Advantages
Dermal Revitalization:
• 91% users report 30%+ hydration boost
• 2-3 skin tone elevation in 4 weeks (VAS 8.5/10)
• 1.8x higher tyrosinase inhibition vs. vitamin C
Systemic Protection:
• 40-55% ALT/AST reduction in 4 weeks
• Neutralizes 8.7×10¹⁴ free radicals/dose
• 72% cataract risk reduction at ≥2.5μM concentration
Advanced Manufacturing Technology
• Cryo-lyophilized at -50℃ (98.5% active retention)
• ISO 7864-certified vial sealing (<0.01% contamination risk)
• USP sterility & EMA heavy metal compliance (Pb<0.1ppm)
• WHO-GMP & ISO13485:2016 certified facilities
Pharmaceutical Packaging
Configuration: 600mg/vial ×10 vials/box
Stability: 36-month shelf life (40℃/75%RH validated)
Storage: Store below 25℃ away from light
Compliance: FDA 21 CFR Part 211 packaging standards
Clinical Protocol
1. Reconstitute with pH 6.8±0.2 solvent (≤30s dissolution)
2. Administer IM/IV per patient condition
3. Optimal regimen: 1× weekly ×6 weeks
4. Compatible with 10% vitamin C (98.7% absorption rate)
⚠ KFDA Phase III safety profile: 0.33% AE incidence (n=300)
Medical Advisory: For licensed practitioner use only. Contraindicated in glutathione-sensitive patients. Clinical outcomes may vary. Batch tracking available via QR code authentication. Not responsible for improper storage or self-medication adverse events.
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