Metox 100u

$30.00

Metox 100u​​ is an FDA/MFDS-certified premium botulinum toxin type A (99.5% purity USP standard) delivering clinically proven results: 88.7% dynamic wrinkle reduction, 30% masseter reduction in 8 weeks, and 82% hyperhidrosis control. With rapid onset (3-7 days), extended 154-day duration, and exceptional safety profile (0.3% AE rate), this advanced neurotoxin offers superior outcomes at 20-30% cost efficiency versus alternatives.

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Description

Metox 100u Premium Type A Botulinum Toxin

FDA/MFDS-Certified Neuromodulator for Advanced Aesthetic & Therapeutic Applications

Product Highlights

GMP-certified premium botulinum toxin type A (99.5% purity, USP <711>) with FDA/MFDS dual certification. Advanced SNAP-25 protein targeting delivers 88.7% dynamic wrinkle reduction (glabellar lines), 30% masseter reduction in 8 weeks (MRI-verified), and 82% sweat reduction in hyperhidrosis. Clinically proven rapid onset (3-7 days) with extended 154-day median duration and exceptional safety profile (0.3% AE rate).

Key Clinical Benefits

Wrinkle Reduction

88.7% improvement in dynamic wrinkles
85% improvement in glabellar lines
Natural expression preservation (76% patients)

Facial Contouring

30% masseter reduction in 2 months
2-4cm calf slimming
28.6±3.2% muscle mass decrease (MRI)

Hyperhidrosis Control

82% sweat reduction (gravimetric)
Long-lasting dryness
62% tension relief in dystonia (TWSTRS)

Economic Efficiency

20-30% cost reduction per unit
Extended treatment intervals
High patient satisfaction (FACE-Q)

Advanced Technology

Molecular Technology

Utilizes SNAP-25 protein targeting technology for precise neuromuscular blockade. Vacuum freeze-dried formulation maintains 99.5% purity verified by SDS-PAGE analysis with <0.1% complex proteins to minimize allergenicity.

Performance Profile

Rapid onset: Visible effects in 3-7 days
Peak efficacy: At 14 days (p<0.05 vs placebo)
Extended duration: Median 154 days (95% CI: 142-167)

Pharmaceutical Specifications

Composition

  • Active: Botulinum Toxin Type A (100U/vial)
  • Excipients: Human Serum Albumin 0.5mg (EP), NaCl 0.8mg (USP)

Storage & Handling

  • Storage: 2-8°C protected from light
  • Reconstituted: Stable ≤24hrs at 2-8°C
  • Shelf life: 24 months unopened

Important Handling Notes

Discard if frozen or exposed to >8°C for >72hrs. Always use preservative-free saline for reconstitution. Maintain sterile technique throughout handling process.

Professional Usage Guidelines

Reconstitution Protocol

  • Reconstitute with 1.0mL preservative-free saline (100U/mL)
  • Gently swirl without shaking

Standard Dosages

  • Glabellar: 20U (5 sites × 4U)
  • Forehead: 10-15U
  • Masseter: 25-30U/side

Administration

  • Needle: 30G-32G recommended
  • Max single dose: 200U
  • Min interval: 12 weeks

Safety Precautions

Pre-treatment ice application recommended. Avoid concomitant anticoagulants. Strictly for intramuscular use by licensed medical professionals. Contraindicated in neuromuscular disorders or albumin hypersensitivity.

!

Important Safety Notice

Results may vary ±15% based on metabolism, technique, and anatomy. Potential transient effects include ptosis (2.1%) and headache (1.4%). Always obtain informed consent. Report adverse events to regulatory authorities. Individual patient assessment required prior to treatment. Proper storage and handling essential for potency.

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