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Botulax contains 200 units (U) of Clostridium botulinum toxin type A, albumin (human) and sodium chloride in a sterile, vacuum-dried from without a preservative. Botulinum toxin type A neutroxin: purified from Clostridium botulinum type A Albumin: Human serum albumin, bulking and stabilizing agent and adhesion reducer. KP grade NaCl: Bulking agent and keeping isotonicity during formulation KP grade Developmental status: 2007.5: reported nonclinical study 2008.3: reported clinically study Phase l 2009.7: Finished Phase lll clinically study Characteristics of Botulax: Higher specific activity than those of other company’s botulinum toxin products by improving lyophilization process Facility: GMP approved by KFDA Composition

Description:

It appears a lyophilized white powder for injection in a colorless transparent vial

Mode of action

• Botulinum Toxin Type A blocks signals from the nerves to the muscles.
• The injected muscle can no longer contract, which causes the wrinkles to relax and soften.
• It is most often used on forehead lines, crow’s feet (lines around the eye) and frown lines.

Features and Benefits

• Botulax guarantees high patient satisfaction.
• Potency variation is strictly controlled to within 191-215 units/ vial, more stringent than the legally required range.
• Size of toxin complex is 900kDa, minimize spread of botulinum toxin outside of the injection site.
• Such large and homogeneous size of the toxin complex ensures precise and uniform effect at the time of injection, guaranteeing high patient satisfaction with Botulax

The package includes a glass ampoule in which the powder is placed under pressure. Sometimes the ampoule may seem empty. For use, dilute the powder in the ampoule with saline. For 100 units, add 2.5 ml of saline, for 200 units – 5 ml of saline.