Kaimax 200 Units

Kaimax 200 Units

Introducing Kaimax 200 Units. Product Description in Depth:

[COMPOSITION]: 1vial includes

Clostridium botulinum toxin type A (in-house)…….. 200 Units (U) Human serum albumin (EP)…………….1.0 mg Sodium chloride (USP)…………….1.8 mg

[DESCRIPTION]

When diluted with normal saline, the white or light-yellow dried powder in a colourless and clear glass vial should turn into a colourless transparent or light-yellow liquid.

[INDICATIONS AND APPLICATIONS]

Kaimax 200 Units (botulinum toxin type A injection) is intended in adult patients aged 19 to 65 years for the temporary relief of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activation.

[ADMINISTRATION AND DOSE]

PREPARATION AND DILUTION METHODS:

Dilute with sterile, preservative-free 0.9% sodium chloride injection to 100U/2.5ml (4U/0.1ml).

Dilution method: Each Kaimax 200 Units vial should be reconstituted with sterile, preservative-free saline. The diluent of choice is 0.9% sodium chloride injection. Fill a syringe with the required amount of diluent. Slowly inject the diluent into the vial because this medicine will be denatured if there is froth or other agitation. If the vial was not filled with diluent while under vacuum, discard it. On the label, write the date and time of dissolution, and allow it to be administered within 24 hours of dissolution.

Kaimax 200 Units should be stored in a refrigerator at 2-8°C after reconstitution. When Kaimax is dissolved, it should be colourless and transparent, with no foreign substance present. Prior to delivery, parenteral formulations should be checked for foreign contaminants and discolouration. Because this medicine and diluent include no preservatives, it is not recommended to utilise a single vial for more than one patient.