JUVEDERM® SKINVIVE
$359.00
/unitProduct details
- Brand:
- JUVEDERM®
- Manufacturer:
- Allergan Inc.
- Active Substance(s):
- HYALURONIC ACID (HA), LIDOCAINE
- Strength:
- 12mg/ml
- Pack size:
- 2 x 1ml pre-filled syringe(s) + 4 needles 32G-1/2"
Product description
Juvederm® Skinvive is an FDA-approved hyaluronic acid intradermal microdroplet injectable indicated to improve cheek skin smoothness in adults over 21. It is formulated as a smooth HA gel with lidocaine and is intended for administration by trained aesthetic professionals in licensed clinical settings. For ordering guidance, contact Doctor Medica customer service.
Tier
| Packs | Discount (%) | For Each |
|---|---|---|
| 1 - 5 | — | $359.00 |
| 6 - 10 | 2.79 % | $349.00 |
| 11 - 20 | 4.18 % | $344.00 |
| 21+ | 5.57 % | $339.00 |
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Product description
What is Juvederm® Skinvive?
Juvederm® Skinvive is an injectable dermal filler from Allergan Aesthetics, an AbbVie company. The FDA lists the product as SKINVIVE by JUVÉDERM, with approval dated May 11, 2023, under PMA supplement P110033/S059.
It contains cross-linked hyaluronic acid, BDDE crosslinking agent, and 0.3% lidocaine to reduce discomfort on injection. Unlike traditional fillers, Skinvive is placed intradermally using a microdroplet technique to improve cheek skin smoothness rather than restore volume or contour.
Product Specifications
- Active ingredient: Hyaluronic acid (HA), modified/cross-linked
- Strength: 12 mg/mL HA with 0.3% w/w lidocaine
- Product type: Injectable gel implant; HA microdroplet injectable
- Format: Prefilled syringe for intradermal injection
- Manufacturer: Allergan Aesthetics, an AbbVie company
- Regulatory status: FDA-approved in 2023 for cheek skin smoothness in adults over 21
- CAS number: Hyaluronic acid CAS 9004-61-9; lidocaine CAS 137-58-6
- Molecular type: Cross-linked hyaluronic acid glycosaminoglycan gel
- Storage: 2–25°C; do not freeze; protect from direct sunlight
- Intended use: Licensed aesthetic medicine practitioners only
How Is Juvederm® Skinvive Formulated?
Skinvive uses the VYC-12L formulation: hyaluronic acid at 12 mg/mL, cross-linked with BDDE (1,4-butanediol diglycidyl ether). BDDE cross-linking creates covalent bonds between HA chains, increasing the gel’s resistance to enzymatic degradation and extending its persistence in the dermis compared with non-cross-linked HA solutions.
The formulation is designed for intradermal placement rather than subdermal or supraperiosteal injection. Its lower gel stiffness and cohesivity, which is compared with volumizing VYCROSS-platform fillers, make it specifically suited to the superficial dermal layer, where it improves tissue hydration and cheek skin smoothness without producing structural augmentation.
In CE-marked markets, the same base formulation is available without lidocaine as Juvederm® Volite, with broader indications approved for additional facial and body areas. Practitioners should verify local prescribing information and current regulatory status before use. (Regulatory information current as of May 2026.)
How Long Does Juvederm® Skinvive Last?
Juvederm® Skinvive is used in licensed aesthetic settings for adults seeking improvement in cheek skin smoothness, particularly where roughness, fine textural irregularity, or reduced dermal hydration are the primary concerns.
In the pivotal clinical trial (Alexiades M et al., Dermatol Surg. 2023), Skinvive demonstrated a statistically significant improvement in cheek skin smoothness in a randomized, multicenter, evaluator-blinded, controlled study.
- The treatment results sustained for at least 6 months. 57.9% of treated participants achieved at least a 1-point improvement on the Allergan Cheek Smoothness Scale at one month compared with 4.5% in the no-treatment control group.
- 6% maintained this response at six months.
Moreover, Skinvive by Juvederm® reviews should be based on published clinical evidence rather than anecdotal or social media sources. Patient-reported outcome data also showed marked improvements in satisfaction with skin hydration, radiance, and overall appearance at one month, sustained through six months.
However, safety and effectiveness have not been established for treatment areas outside the cheeks, and use should follow approved labeling. Other Juvederm® products have separate indications for volume, contouring, or wrinkle correction and should not be used interchangeably with Skinvive without reviewing their specific labeling.
How Is Juvederm® Skinvive Administered?
Juvederm® Skinvive is administered by intradermal microdroplet injection into the cheeks using an ultrafine needle by a trained aesthetic practitioner. Injection depth, volume, and distribution pattern are determined by the treating clinician based on patient assessment and labeling guidance. Sessions typically last 30–45 minutes, with repeat treatments at 6-month intervals to maintain skin smoothness.
Treatment should be postponed if active skin sores, rashes, cysts, infection, or inflammatory skin lesions are present at the intended injection site. Practitioners should advise patients to report vision changes, stroke-like symptoms, skin whitening, or unusual pain during or shortly after treatment, as these may indicate intravascular injection.
What Are the Side Effects and Drug Interactions?
Common injection site reactions from injectables like Skinvive are (generally mild to moderate; most resolve within 30 days):
- Redness, swelling, and bruising
- Tenderness, pain, and discomfort
- Firmness, lumps, or bumps
- Discoloration and itching
This treatment can also carry serious risks (rare but clinically significant):
- Vascular occlusion, which is the unintentional intravascular injection may cause vision abnormalities, blindness, stroke, tissue necrosis, or permanent scarring
- Delayed inflammatory reactions
- Hypersensitivity events in patients with severe allergies, lidocaine sensitivity, or prior HA filler reactions
It’s vital for practitioners to discuss the following drug interactions and contraindications prior to treatment:
- Aspirin, NSAIDs, or anticoagulants: Increased bruising and bleeding risk
- Immunosuppressive therapy: Increased infection risk
- Recent or planned laser treatments, chemical peels, or resurfacing procedures: Pose a risk of inflammatory reaction
- Active skin infection or inflammation at the injection site: Postpone treatment if any of these are present
Juvederm® Skinvive Availability and Access
Juvederm® Skinvive is a prescription medical device and must be sourced through licensed medical, aesthetic, or pharmaceutical channels. Access requirements vary by country, distributor, and professional eligibility. Practitioners should verify current regulatory status, local approved indications, and storage requirements before procurement. For guidance on product availability, contact Doctor Medica customer service.
Explore the complete catalog to buy JUVEDERM® online with wholesale options available for professional use.
Written by Doctor Medica’s Editorial team
The content on this page has been written and fact-checked in accordance with our Editorial Policy. Clinical claims are sourced from peer-reviewed literature, regulatory documentation, and manufacturer specifications. Where citations are provided, it is always in accordance to our editorial standards.
FAQ
Skinvive by Juvederm® is an FDA-approved hyaluronic acid injectable gel from Allergan Aesthetics, an AbbVie company. It is administered via an intradermal microdroplet technique and is indicated to improve cheek skin smoothness in adults aged 21 and older. It is not intended for volumizing, lifting, or contouring.
Clinical data from the pivotal trial showed that Skinvive improved cheek skin smoothness with effects lasting at least six months. Maintenance or repeat treatment may be considered based on patient response, clinical assessment, and labeling guidance.
In the pivotal clinical study, Skinvive produced statistically significant improvement in cheek skin smoothness at one month compared with no treatment. 57.9% of treated participants achieved at least a 1-point improvement on the Allergan Cheek Smoothness Scale at one month, and 55.6% maintained this response at six months.
Skinvive by Juvederm® is designed for intradermal hydration and skin smoothness, not facial volumizing, lifting, or contouring. Unlike traditional Juvederm® fillers, it is placed as microdroplets within the dermis and is FDA-approved specifically for improving cheek skin smoothness.
Yes. Skinvive by Juvederm® received US FDA approval in 2023 for intradermal injection to improve the smoothness of cheek skin in adults aged 21 and older. It is the first and only hyaluronic acid intradermal microdroplet injection approved in the US for this specific indication.
- Alexiades M, Palm MD, Kaufman-Janette J, et al. A Randomized, Multicenter, Evaluator-blind Study to Evaluate the Safety and Effectiveness of VYC-12L Treatment for Skin Quality Improvements. Dermatol Surg. 2023;49(7):682-688. doi:10.1097/DSS.0000000000003802
- Chiu A, Montes JR, Munavalli G, Shamban A, Chawla S, Abrams S. Improved Patient Satisfaction With Skin After Treatment of Cheek Skin Roughness and Fine Lines With VYC-12L: Participant-Reported Outcomes From a Prospective, Randomized Study. Aesthet Surg J. 2023;43(11):1367-1375. doi:10.1093/asj/sjad111
- Niforos F, Ogilvie P, Cavallini M, et al. VYC-12 Injectable Gel Is Safe And Effective For Improvement Of Facial Skin Topography: A Prospective Study. Clin Cosmet Investig Dermatol. 2019;12:791-798. Published 2019 Oct 24. doi:10.2147/CCID.S216222
- Kablik J, Monheit GD, Yu L, Chang G, Gershkovich J. Comparative physical properties of hyaluronic acid dermal fillers. Dermatol Surg. 2009;35 Suppl 1:302-312. doi:10.1111/j.1524-4725.2008.01046.x
- US Food and Drug Administration. SKINVIVE by JUVÉDERM – P110033/S059. US Food and Drug Administration. May 11, 2023. Updated July 10, 2023. https://www.fda.gov/medical-devices/recently-approved-devices/skinvive-juvederm-p110033s059
