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Injectables

Skinvive by Juvéderm Wins FDA Approval for Neck — What's in Your Filler Mix Now

AbbVie's newest indication expands the Juvéderm franchise into a high-complaint zone; implications for your injectable protocol and patient conversation.

Photo: Gustavo Fring · Pexels

Allergan Aesthetics has secured FDA approval for Skinvive by Juvéderm for the improvement of neck appearance—specifically neck lines and skin texture. This marks the first and only FDA-cleared hyaluronic acid injectable designed specifically for neck treatment, a clinical gap that has forced practitioners to either use off-label filler or refer neck work elsewhere.

First and only FDA-cleared HA injectable designed specifically for the neck.

Skinvive is formulated with a lower concentration of cross-linked HA than traditional Juvéderm volumizers, optimized for the thinner, more mobile skin of the neck and décolletage. The approval rests on data showing sustained improvement in neck lines and skin quality at 12 weeks, with durability extending beyond six months in some patients. For practices already integrated into the Allē loyalty ecosystem, this represents a new SKU to stock and a new revenue stream—though neck treatment typically commands lower per-unit pricing than facial volumization. The real play: patient retention and case expansion in an area where competitors (Galderma, Revance) have not yet secured comparable cleared indications.

Source: original report ↗

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