Verified Clinical Specifications | Licensed Practitioners Only
Kaimax 100U Botulinum Toxin Type A
Active Substance
• Clostridium Botulinum CBFC26
• 150 kDa Neurotoxin Complex
• 99.8% Toxin Purity
Formulation Data
• 100 Mouse LD50 Units /
• 0.5 mg HSA (EP Grade)
• 0.9 mg NaCl (USP Grade)
Pharmacokinetics & Efficacy
Immunogenicity Profile
<0.5ng protein/
Endotoxin: ≤0.03 EU/
Action Timeline
Initial Onset: 3-5 days
Therapeutic Peak: 14 days
Metabolism
Duration: 120-150 days
pH Level: 6.8 – 7.4
Standard Reconstitution Protocol
1. Diluent Specification
Inject 2.5ml of 0.9% unpreserved Sodium Chloride. Yields concentration of 4.0U per 0.1ml.
2. Mechanical Handling
Utilize vacuum draw. Employ gentle inversion. Agitation or vortexing causes protein denaturation.
Storage & Stability
• Unopened: 2°C – 8°C (Refrigeration)
• Shelf Life: 36 months from manufacture
• Post-Reconstitution: 2°C – 8°C (Administer within 24 hours)
Regulatory & Contraindication Disclosure:
Kaimax is manufactured by JETEMA Co. in a / facility. Not approved by for retail distribution. Classified as a prescription-only medical device (POM). Supply is strictly restricted to licensed medical practitioners, dermatologists, and certified clinical clinics.
Contraindications: Hypersensitivity to botulinum toxin type A or formulation excipients. Presence of infection at injection site. Known motor neuropathic diseases (e.g., Amyotrophic Lateral Sclerosis, Myasthenia Gravis). Pregnancy or active lactation.

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