HITOX 200U Clinical Specification
Purified neurotoxin complex (900kDa) derived from Clostridium botulinum Hall strain. Kquality-assured clinical equivalence. biomanufacturing facility.
FOR MEDICAL PROFESSIONALS ONLY
Pharmacokinetics
Onset: 72-120 hours post-administration
Peak Efficacy: 14 days
Duration: 16-24 weeks (dose-dependent)
Diffusion: 0.6-1.2cm² target radius
99.8% Integrity
Biochemical Profile
Active Toxin: 200 Units Botulinum Toxin Type A (900kDa)
Excipient 1: 0.5mg Pharmaceutical-Grade Human Serum Albumin (HSA)
Excipient 2: 0.9mg Sodium Chloride (Isotonic Buffer)
Immunogenicity: ≤0.1% resistance risk in Phase III trials
Vacuum-Drying Stabilization
Proprietary lyophilization methodology ensures residual moisture remains <0.1%. Prevents protein denaturation during transit. Shelf-life validated at 36 months under controlled 2-8°C (36-46°F) refrigeration.
Clinical Protocol
Reconstitute with 5.0mL preservative-free 0.9% sterile saline to yield 4.0U/0.1mL.
Utilize 30G-32G microneedle. Administer immediately post-reconstitution.
Maximum recommended cumulative dose: 200U within a 30-day period.
Strictly avoid diffusion into levator palpebrae superioris and zygomaticus major.
⚠️ Contraindications & Medical Review
Contraindicated in patients with known hypersensitivity to any formulation component, myasthenia gravis, or Eaton-Lambert syndrome. Clinical data parameters verified against published multi-center double-blind Phase III trials. Distribution and administration strictly regulated to licensed medical physicians and board-certified dermatologists/plastic surgeons.

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