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HITOX 200U Stabilized Neurotoxin Complex (200 Units/)

$42.80

HITOX 200U Professional-Grade Botulinum Toxin Type A is an quality-assured neurotoxin with 95% purity, clinically proven to reduce dynamic wrinkles within 72 hours (peak efficacy: 14 days). manufacturing ensures 24-month stability, ≤0.35% HSA content, and 0.9% adverse event rate. Features 0.1% immunogenicity risk and 4-6 month duration. For licensed practitioners only. Store at 2-8°C. Supported by 98% patient satisfaction in clinical studies.

SKU: 7933b56e60c6-23af-4be1-a6c3-dd2e3ae278cd Categories: ,
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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

01.

Reconstitute with 5.0mL preservative-free 0.9% sterile saline to yield 4.0U/0.1mL.

02.

Utilize 30G-32G microneedle. Administer immediately post-reconstitution.

03.

Maximum recommended cumulative dose: 200U within a 30-day period.

04.

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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