•Do not inject into blood vessels. Introduction of these products into the vasculature may lead to embolization, occlusion of the vessels, ischemia, or infarction. Take extra care when injecting soft-tissue fillers; for example, inject the product slowly and apply the least amount of pressure necessary. Rare, but serious, adverse events associated with the intravascular injection of soft-tissue fillers in the face have been reported and include temporary or permanent vision impairment, blindness, cerebral ischemia or cerebral hemorrhage leading to stroke, skin necrosis, and damage to underlying facial structures. Immediately stop the injection if a patient exhibits any of the following symptoms: changes in vision, signs of a stroke, blanching of the skin, unusual pain during or shortly after the procedure. Patients should receive prompt medical attention and, possibly, evaluation by an appropriate healthcare professional specialist should an intravascular injection occur
•Product use at specific sites in which an active inflammatory process (skin eruptions such as cysts, pimples, rashes, or hives) or infection is present should be deferred until the underlying process has been controlled

•In order to minimize the risk of potential complications, these products should only be used by healthcare professionals who have appropriate training, experience, and knowledge of facial anatomy
•Healthcare professionals are encouraged to discuss the potential risks of soft-tissue injections with their patients prior to treatment and ensure that patients are aware of signs and symptoms of potential complications
•The safety and effectiveness for the treatment of anatomic regions other than the mid-face with JUVÉDERM^® VOLUMA™ XC; facial wrinkles and folds with JUVÉDERM^® Ultra XC, JUVÉDERM^® Ultra Plus XC, and JUVÉDERM^® VOLLURE™ XC; and the lips and perioral area with JUVÉDERM^® Ultra XC and JUVÉDERM^® VOLBELLA™ XC have not been established in controlled clinical studies
•As with all transcutaneous procedures, dermal filler implantation carries a risk of infection. Follow standard precautions associated with injectable materials
•The safety for use during pregnancy, in breastfeeding females, and in patients with known susceptibility to keloid formation, hypertrophic scarring, and pigmentation disorders has not been studied
•The safety for use of JUVÉDERM^® VOLUMA™ XC in patients under 35 or over 65 years, JUVÉDERM^® Ultra XC and JUVÉDERM^® Ultra Plus XC in patients under 18 years, and JUVÉDERM^® VOLLURE™ XC and JUVÉDERM^® VOLBELLA™ XC in patients under 22 years has not been established
•Use with caution in patients on immunosuppressive therapy
•Patients who are using products that can prolong bleeding (such as aspirin, nonsteroidal anti-inflammatory drugs, and warfarin) may experience increased bruising or bleeding at treatment sites
•If laser treatment, chemical peel, or any other procedure based on active dermal response is considered after treatment, or if these products are administered before the skin has healed completely, there is a possible risk of an inflammatory reaction at the treatment site
•Patients who experience skin injury near the site of implantation may be at a higher risk for adverse events
•The safety of JUVÉDERM^® VOLUMA™ XC injectable gel for use in patients with very thin skin in the mid-face has not been established
•Patients may experience late onset nodules with use of dermal fillers, including JUVÉDERM^® VOLUMA™ XC
•Patients may experience late onset adverse events with use of dermal fillers