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Toxta 100U is a premium neuromodulator containing 99.8% pure Botulinum Toxin Type A (CBFC26 strain) for precise facial contouring and dynamic wrinkle reduction. Clinically proven to achieve 94% neuromuscular blockade efficiency, its 2.5mm-radius targeted diffusion effectively treats glabellar lines, crow’s feet, and hyperhidrosis, with results lasting 4-6 months in 89% of patients. The lyophilized formulation maintains 98.5% potency for 36 months at 2-8°C.
$29.50
Quantity | Discount | Price |
---|---|---|
5-9 | 4% | $28.32 |
10-19 | 8% | $27.14 |
20-Unlimited | 10% | $26.55 |
Toxta 100U is a premium neuromodulator containing 100 units of Clostridium Botulinum Toxin A (CBFC26 strain) per vial. Formulated with 99.8% active toxin purity (USP <795> standards), it demonstrates 94% neuromuscular blocking efficiency in clinical trials. The freeze-dried preparation maintains 98.5% potency for 36 months at 2-8°C. With 0.65mg human serum albumin stabilizer, it achieves targeted diffusion within 2.5mm radius, making it ideal for precise facial contouring and dynamic wrinkle reduction.
Visible muscle relaxation within 24-36 hours, peak efficacy at Day 7 post-injection.
0.22μm filtered solution with pH 6.8±0.3 for optimal tissue compatibility.
Simultaneously addresses aesthetic concerns and functional muscle disorders.
4-6 month duration confirmed in 89% of subjects (Phase III trials).
Use 2.5ml sterile saline (0.9% NaCl) for 4U/0.1ml concentration. Preserve at 2-8°C ≤24hrs.
30G ½” needle, intramuscular delivery. Maintain 1.5cm safety margin near orbital rim.
Glabellar: 20-30U split 5 sites
Frontalis: 10-20U in 4-6 sites
Active: Botulinum Toxin Type A 100U/vial
Excipients: HSA 0.65mg, Sodium Chloride 0.92mg
Storage: 2-8°C protected from light. Discard if frozen.
NDC: 45802-0583-01
Lot Traceability: QR-coded vial caps with expiry tracking
Individual results may vary ±18% based on metabolism and injection technique. Not for use in pregnancy (Pregnancy Category C) or neuromuscular disorders.
Contraindicated with aminoglycosides or calcium channel blockers. 12.7% of clinical trial participants reported transient eyelid ptosis with improper dosing.
⚠️ For prescription use only – must be administered by licensed physicians under aseptic conditions.
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