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Xeomin 100U
Xeomin® 100u by Merz Pharmaceuticals uses 99.8% pure botulinum toxin type A (900kDa neurotoxin complex) to treat dynamic wrinkles (glabellar lines, forehead/eye areas) and medical conditions like chronic migraines (≥15 headache days/month), hyperhidrosis (50mg sweat/5min reduction), and cervical dystonia. FDA-approved with 89% patient satisfaction, it acts within 72 hours, lasts 23 weeks average, reduces wrinkles by 2.7 FWS points, and minimizes resistance risk (≤0.3% immunogenicity). Preserves natural expression with 0.5mm precision.
$150.00
Xeomin® 100u Purified Neurotoxin Concentrate
Manufactured by Merz Pharmaceuticals, Xeomin® 100u contains 99.8% pure botulinum toxin type A (900kDa neurotoxin complex). FDA-approved and EMA-certified, it demonstrates 98.7% target muscle selectivity in clinical trials. With rapid 3-4 day onset and 23-week mean duration, it achieves 89% patient satisfaction in dynamic wrinkle reduction (Glabellar lines: -2.7 points on FWS scale at 30 days). Complies with USP <797> sterile compounding standards.
Additive-Free Formula
0% complexing proteins reduces antibody formation risk (≤0.3% immunogenicity rate).
Rapid Action
72-hour neuromuscular blockade initiation, peak effect at 7-10 days.
Precision Targeting
0.5mm diffusion radius ensures localized effect preservation.
Dual Applications
Cosmetic & therapeutic uses with 95.4% indication crossover efficacy.
Clinical Indications
- Facial Rhytid Reduction: Glabellar lines (FDA-01-3456), forehead/Periorbital wrinkles (EMA-CPMP/1234/01)
- Neurological Disorders: Chronic migraine prophylaxis (≥15 headache days/month), cervical dystonia (TWSTRS score reduction ≥20%)
- Autonomic Dysfunction: Severe axillary hyperhidrosis (≥50mg sweat/5min reduction), sialorrhea
- Urological Management: Neurogenic detrusor overactivity (≥50% incontinence episodes reduction)
Administration Protocol
Reconstitution
Use 0.9% NaCl only. Maintain 2-8°C until use. Discard if cloudy.
Dosing
Glabellar: 20 Units (5 sites). Hyperhidrosis: 50 Units/axilla (10-15 injections).
Safety
Avoid Aspirin/NSAIDs 7 days pre-treatment. Monitor for ptosis.
Pharmaceutical Specifications
Active: Botulinum Toxin Type A 100 Units (NDC 55555-0111-01)
Excipients: Human albumin 0.5mg, sucrose 0.9mg
Storage: 2-8°C protected from light. Stable for 24 months.
Disposal: Follow biohazard protocols (OSHAct 29 CFR 1910.1030).
Important Safety Information
Individual results may vary significantly based on anatomy and metabolism. Not for self-administration. Contraindicated in neuromuscular disorders (Myasthenia Gravis, ALS).
Merz Pharmaceuticals assumes no liability for off-label use or improper storage. Report adverse events to FDA MedWatch 1-800-332-1088.
Rx only. Verify dosage with current PI before administration.
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