Allergan Botox 50 and 100 units: active substance, excipients, indications according to the Dutch CBG product information and professional terms. For qualified professionals only.
Open the product page for the exact version, pack and product information.
Botox from Allergan is a prescription-only medicine containing botulinum toxin type A, supplied as a powder for solution for injection with human albumin and sodium chloride as excipients. The Dutch CBG product information describes medical indications, including blepharospasm, cervical dystonia, focal spasticity, chronic migraine, overactive bladder and severe primary axillary hyperhidrosis; it does not describe an indication for cosmetic wrinkle reduction. The product information in your country may differ. This information is intended exclusively for qualified healthcare professionals.
The catalogue lists Allergan Botox 50 units and 100 units separately. Check the exact product page and the documentation of the version concerned. Units of different botulinum toxin products are not interchangeable; a unit statement is not treatment advice.
Check the full product identity, applicable licences, origin, batch/lot data, expiry date and official documentation. A brand name on a website is not proof of manufacturer authorisation.
They are separate catalogue entries. Check the stated version and pack on the product page and in the official product documentation. Neither dose nor interchangeability can be derived from this.
The responsible qualified professional, practice details, the exact version and the delivery country. Authorisation, product status and delivery terms are checked separately.
A listing on this website is not proof of a marketing authorisation, official manufacturer authorisation or permitted delivery to your country. A professional account does not in itself authorise the purchase of medicines. Have the exact product status, documentation and terms checked in advance.
Always check the official product documentation and applicable professional regulations.
Original products with documented origin, traceable batch/lot details and intact factory seals. CE marking is stated only for the relevant CE-marked medical devices and in accordance with product documentation. Medicines are subject to the product status and official information applicable in the destination country.
For products requiring refrigerated transport, Cosmoface guarantees cold transport in accordance with the applicable product requirements.
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Cosmoface supplies 100% original products with documented origin and batch traceability. We do not supply products without the required origin and product documentation. Our medical devices are CE-marked under the applicable European regulations. Medicines are subject to the relevant registration and official product information.
Original factory seals remain intact, including double seals where used by the manufacturer. Your practice receives the product in its original, unopened packaging.