A Study to Evaluate The Impact on Skin Quality Attributes by Juvederm® Volite Injection on Healthy Volunteers

* Healthy participants * Participants with Fitzpatrick skin type II or III * Participant willing to receive Juvéderm® VOLITE in the forearms and agrees to complete all study required procedures, including having 6 cutaneous punch biopsies taken in the forearms and blood drawn (Human immunodeficiency virus \[HIV\], B and C hepatitis analysis at screening) * Written informed consent and data privacy consent obtained

* Pregnant or nursing woman or planning a pregnancy during the study * Participant participating to another research on human beings or being in an exclusion period for a previous study * Intensive exposure to sunlight or ultraviolet (UV)-rays within the previous month and foreseen during the study * Participant having other resorbable filling product injections, a laser treatment, an ultrasound-based treatment, radiation treatment, a dermabrasion, a surgery, a deep chemical peeling or other ablative procedure on the studied zones within the past 12 months prior to study start * Participant with subcutaneous retaining structure on the studied zones (meshing, threads, gold strand) * Participant having received injections of permanent or semi-permanent filling products in the studied zones * Participant under anti-coagulant treatment or treatment liable to interfere with the healing process or hemostasis, during the previous month and during the study * Participant receiving or is planning to receive anti-inflammatory drugs (oral/injectable corticosteroids or Nonsteroidal anti-inflammatory drugs (NSAIDs), e.g., aspirin, ibuprofen), or other substances known to increase coagulation time (herbal supplements with garlic or ginkgo biloba, etc) for 10 days prior to study treatment and 3 days after * Participant under immunosuppressive therapy