SKINVIVE™ by JUVÉDERM®
Professional Grade Injectable
The first and only FDA-approved hyaluronic acid (HA) intradermal microdroplet injection in the US. Engineered specifically to improve skin smoothness and hydration of the cheeks, providing a lasting glow without altering facial volume or expression.
12 mg/mL
HA Concentration
0.3%
Lidocaine HCl
Clinical Specification
Indication: Intradermal injection for cheek skin smoothness.
Device Class: III Medical Device.
Sterile: Steam sterilized gel.
Clinical Efficacy & Longitudinal Data
Primary Endpoint Met: In a pivotal clinical study, 63% of patients maintained a ≥1-point improvement on the Allergan Cheek Smoothness Scale (ACSS) at month 6, compared to 28% in the control group.
High Glow Satisfaction: At 6 months, 91% of participants reported satisfaction with how refreshed and healthy their skin appeared. Secondary endpoints confirmed significant improvements in skin hydration and radiance.
Microdroplet Technology & Aquaporin-3
Unlike traditional fillers that provide structural volume, SKINVIVE™ uses Microdroplet Intradermal Injection. The cross-linked HA formulation integrates within the dermal layer to increase Aquaporin-3 (AQP3) expression—a key protein responsible for water and glycerol transport in the skin.
This mechanism optimizes internal hydration levels and reinforces the extracellular matrix, leading to improved tactile smoothness and biological skin quality.
Packaging Specifications
2 x 1.0 mL Prefilled Syringes
32G ½” Needles Included
Professional Application Protocol
01
Site Preparation
Aseptic cleansing of the mid-face and malar regions. Topical anesthesia is optional due to integrated 0.3% lidocaine.
02
Injection Technique
Multiple microdroplet injections (0.01 to 0.05 mL per point) delivered into the mid-to-deep dermis, spaced 0.5 to 1 cm apart.
03
Post-Treatment
Gentle palpation to ensure even distribution. Avoid high-intensity exercise and ethanol consumption for 24 hours post-procedure.
Safety Compliance & Contraindications
Prescription Use Only: This product is restricted for sale to and use by licensed healthcare professionals only. Verification of medical credentials is required prior to shipping.
Contraindications: Do not administer to patients with a history of severe allergies (anaphylaxis) or allergies to Gram-positive bacterial proteins or lidocaine.
Adverse Reactions: Common side effects observed in clinical trials include redness, swelling, bruising, and tenderness at the injection site, typically resolving within 7 days.
Authentication: All units are traceable via batch number and expiry date provided on the external packaging. Guaranteed authentic JUVÉDERM® product line.

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