This material refers to the product certified under Regulation (EU) 2017/745 (MDR). Legacy versions of the product remain available. For full product information and the Instructions for Use (IFU), visit: www.galderma.com/library.
Always consult your healthcare professional for individualized treatment recommendations and to discuss important safety information and risks associated with the use of the products.
References
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Job code: UKI-SCU-2600004 Date of Preparation: March 2026
AE Statement: Adverse events should be reported.
For the UK, Reporting forms and information can be found at or search for Yellow Card in the Google Play or Apple App Store.
For Ireland, Suspected adverse events can be reported via HPRA Pharmacovigilance, Website: ; Adverse events should also be reported to Galderma (UK) Ltd, Email: , Tel: +44 (0) 300 3035674
Other Disclaimers: ‘Individual results may vary’