revanceaesthetics.comOfficial Site: Revance Aesthetics

Portfolio NEUROMODULATOR Filler Technology PREMIER TRAINING Partnership Journey RESOURCES Award Winning The first and only long-lasting, peptide-powered frown line treatment 1-8* Experience Daxxify® *At least 50% of patients in SAKURA 1 and SAKURA 2 had none or mild frown lines for 24 weeks (6 months) and 23.9 weeks (6 months) or longer, respectively, per both investigator’s and patient’s assessments. 4 From TIME. © 2023 TIME USA LLC. All rights reserved. Used under license. Our Portfolio Our expertly curated suite of products and services is incredibly innovative in today’s market and serves an unmet need to both our aesthetic provider partners and their clients. THE FUTURE OF AESTHETICS Learn More Please see DAXXIFY ® full Prescribing Information , including Boxed Warning and Medication Guide . The latest innovation in hyaluronic acid fillers The latest innovation in hyaluronic acid fillers Learn More The latest innovation in hyaluronic acid fillers Learn More THE PREMIER INJECTOR TRAINING AND EDUCATION PLATFORM Learn More AwardsRecognition DAXXIFY® DAXXIFY® DAXXIFY® DAXXIFY® DAXXIFY® RHA® COLLECTION WINNER x2 DAXXIFY® DAXXIFY® RHA Redensity™ RHA Redensity™ DAXXIFY® WINNER TWO YEARS IN A ROW DAXXIFY® DAXXIFY® DAXXIFY® DAXXIFY® DAXXIFY® RHA® COLLECTION WINNER TWO YEARS IN A ROW Resources Providing a new level of excellence in training, education, marketing, practice development, and more. Learn More JOURNEY Leading With Market Innovation Revance Aesthetics is meeting unmet market needs with cutting-edge innovation and first-of-its kind products. Our journey is as unique as we are. Learn More Partnership Our approach is different and focused on delivering growth opportunities for our aesthetic provider partners. We prioritize your practice and your success every step of the way. Learn More Join us on instagram In the media 2023 InStyle® Best Beauty Buys logo © 2023 TI Gotham, Inc., a Dotdash Meredith company. Used under license. 2023 Shape® Beauty logo © 2023 Meredith Operations Corporation, a Dotdash Meredith company. Used under license. From TIME. © 2023 TIME USA LLC. All rights reserved. Used under license. WARNING: DISTANT SPREAD OF TOXIN EFFECT The effects of DAXXIFY ® and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. DAXXIFY ® is not approved for the treatment of spasticity or any conditions other than glabellar lines. INDICATION DAXXIFY® (daxibotulinumtoxinA-lanm) injection is an acetylcholine release inhibitor and neuromuscular blocking agent indicated for the temporary improvement in the appearance of moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity in adult patients. IMPORTANT SAFETY INFORMATION Contraindications DAXXIFY® contraindications include hypersensitivity to any botulinum toxin preparation or any of the components in the formulation and infection at the injection site(s). Warnings and Precautions Please refer to Boxed Warning for Distant Spread of Toxin Effect. The potency Units of DAXXIFY® are not interchangeable with other preparations of other botulinum toxin products. Recommended dose and frequency of administration should not be exceeded. Patients should seek immediate medical attention if respiratory, speech or swallowing difficulties occur. Use caution when administering to patients with pre-existing cardiovascular disease. Concomitant neuromuscular disorders may exacerbate clinical effects of treatment. Adverse Reactions The most commonly observed adverse reactions (≥1%) were headache (6%), eyelid ptosis (2%) and facial paresis (1%). Drug Interactions Co-administration of DAXXIFY® and aminoglycoside antibiotics, anticholinergic agents or any other agents interfering with neuromuscular transmission or muscle relaxants should only be performed with caution as the effect of DAXXIFY® may be potentiated. The effect of administering different botulinum neurotoxins during course of treatment with DAXXIFY® is unknown. Use in Specific Populations DAXXIFY® is not recommended for use in children or pregnant women. Please see DAXXIFY® full Prescribing Information , including Boxed Warning and Medication Guide. DAXI-001720.2 PLEASE SEE FULL DIRECTIONS FOR USE RHA® Collection of Fillers Indications The RHA® Collection of resilient hyaluronic acid (HA) fillers includes RHA Redensity™, RHA® 2, RHA® 3 and RHA® 4. RHA Redensity™ is indicated for injection into the dermis and superficial dermis of the face, for the correction of moderate to severe dynamic perioral rhytids in adults 22 or older. RHA® 2 is indicated for injection into the mid-to-deep dermis for the correction of moderate to severe dynamic facial wrinkles and folds, such as nasolabial folds in adults 22 or older. RHA® 3 is indicated for injection into the mid-to-deep dermis for the correction of moderate to severe dynamic facial wrinkles and folds, such as nasolabial folds and is also indicated for injection into the vermillion body, vermillion border and oral commissure to achieve lip augmentation and lip fullness in adults 22 or older. RHA® 4 is indicated for injection in the deep dermis to superficial subcutaneous tissue for the correction of moderate to severe dynamic facial wrinkles and folds, such as nasolabial folds in adults 22 or older. IMPORTANT SAFETY INFORMATION Contraindications Do not use in patients who have severe allergies, marked by a history of anaphylaxis or multiple severe allergies, or in patients with a history of allergies to gram-positive bacterial proteins or local anesthetics of the amide type, such as lidocaine. Do not use in patients with bleeding disorders. Warnings 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, or 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 or infection is present should be deferred until the underlying process has been controlled. Precautions These products should only be used by healthcare professionals who have appropriate training, experience, and knowledge of facial anatomy. Discuss the potential risks of soft-tissue injections with your 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 labeled indications have not been established in controlled U.S. clinical studies. As with all transcutaneous procedures, dermal filler implantation carries a risk of infection. Standard precautions associated with injectable materials should be followed. The safety for use in sites in the presence of other implants, during pregnancy, in breastfeeding females, and in patients with known susceptibility to keloid formation, hypertrophic scarring, and pigmentation disorders has not been studied. Use with caution in patients on...