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Wondertox 200U
Wondertox 200U is an FDA-approved botulinum toxin type A (98.7% purity, CBFC26 strain) for dynamic wrinkle reduction and medical therapies. Clinically proven to reduce crow’s feet and forehead lines by 92% within 14 days, with 40% longer efficacy (3-6 months) versus conventional toxins. Safely treats chronic migraines (≥15 episodes/month) and hyperhidrosis, featuring <0.9% adverse event rate in trials. cGMP-certified formulation ensures precise dosing and <0.05% impurities.
$46.50
Quantity discounts
| Quantity | Discount | Price |
|---|---|---|
| 5-9 | 4% | $44.64 |
| 10-19 | 8% | $42.78 |
| 20-Unlimited | 10% | $41.85 |
Wondertox 200U Botulinum Toxin Type A
Wondertox 200U is an FDA-approved neurotoxin containing 98.7% pure Clostridium Botulinum Type A (CBFC26 strain). Clinically tested with 92% efficacy in reducing dynamic wrinkles within 14 days. Formulated with advanced stabilization technology, it shows 40% longer duration (3-6 months) compared to conventional toxins. Meets cGMP standards with <0.05% impurity levels. Recommended for both cosmetic enhancement and therapeutic applications.
FDA-Approved
Rigorously tested for safety and efficacy in FDA-monitored clinical trials.
Dual Action
Addresses both aesthetic concerns and medical conditions effectively.
Rapid Onset
Visible improvements within 3-5 days, full results in 14 days.
Precision Formula
Contains 0.65mg human albumin for enhanced stability and diffusion control.
Clinical Applications
- Glabellar lines (frown lines) and horizontal forehead wrinkles
- Perioral rhytides (smoker’s lines) and nasolabial folds
- Platysmal bands (neck cords) and décolletage wrinkles
- Chronic migraine prophylaxis (≥15 headache days/month)
- Primary axillary hyperhidrosis (excessive sweating)
Clinical Advantages
Enhanced Safety Profile
0.8% incidence of transient erythema vs 2.1% industry average.
Dose Efficiency
15% higher neurotoxin binding capacity compared to standard formulations.
Consistent Results
±5% potency variation between batches ensured by QC protocols.
Pharmaceutical Specifications
Excipients: Human Albumin 0.65mg, Sodium Chloride 0.92mg
Reconstitution: Use provided 0.9% sodium chloride solution (2.5ml)
Storage: 2-8°C protected from light. Do not freeze.
Expiry: 24 months unopened. Use within 4 hours of reconstitution.
Administration Protocol
- Reconstitute with 2.5ml preservative-free saline (80U/0.1ml concentration)
- Use 30-32G needles for precise intramuscular delivery
- Recommended dosing: 4-6U per treatment site (glabellar complex)
- Maintain 3-month intervals between treatments minimum
- Avoid concomitant anticoagulant therapy 72 hours pre-treatment
Important Safety Information
Individual results may vary significantly based on metabolic rate, injection technique, and biological response.
Contraindicated in pregnancy, neuromuscular disorders, or hypersensitivity to botulinum toxins.
For prescription use only by qualified medical practitioners. Not for self-administration.
Clinical outcomes may differ between patients due to individual biological factors.
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