BIENOX 100u Botulinum Toxin Type A
Medically Reviewed & Validated Data
Source: Phase III Clinical Trials | Standard: ISO 13485 Certified | Grade: Medical Neuromodulator
Therapeutic Efficacy
77% improvement in FWS-30 scale for moderate-to-severe glabellar lines.
Onset Time: 24-72 hours.
Peak Efficacy: 14 days.
Duration: 3-6 months (4.2 months mean duration).
Advanced Cryopurification Data
99.8% Active Toxin Concentration
150kDa Neurotoxin Integrity Maintained
≤0.05ng Hemagglutinin Proteins
pH-stable 6.8±0.3 Formulation (0.9% NaCl)
CLINICAL PROTOCOL
01
Reconstitution
Reconstitute with 0.9% NaCl (2.5ml per 100U vial).
02
Dosage
Inject 0.1ml (4U) per site via Intramuscular (IM) injection.
03
Administration
Apply 5-point glabellar technique. Maximum 20U per session. 90-day interval.
CONTRAINDICATIONS & SAFETY PROTOCOL
Contraindicated for neuromuscular disorders, pregnancy, and lactation. ≤0.3% adverse event probability in controlled environments.
Strictly for administration by licensed medical practitioners holding ≥2 years of neuromodulator experience. Storage required at 2-8°C to maintain 100U ± 5% potency.

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