GaldermaAnnouncesU.S.FDAAcceptanceofRelabotulinumtoxinABiologicsLicenseApplicationResubmission
===2026/2/3 10:03:21===
ed a fast onset of action as early as Day 1 and sustained results for six months for both frown lines and crow’s feet.1,2
RelabotulinumtoxinA (Relfydess™) has been approved in over 20 markets for the treatment of frown lines and crow’s feet, including in the European Union, the United Kingdom, Asia, and Australia. Regulatory applications are continuing to be submitted and assessed by additional authorities globally.
Galderma offers a range of neuromodulator solutions aiming to address every single injector and patient need, and has the heritage, expertise and capability needed to continue bringing this advanced solution to patients and healthcare professionals globally. Today, Galderma is well positioned to be the leader in all aspects of Injectable Aesthetics, having the in-house capabilities to discover, research, develop, manufacture, and market best-in-class products.
About RelabotulinumtoxinA
Pioneered by Galderma, RelabotulinumtoxinA is the first
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