Catalogue identityDataset 2026.08.15.1

Skinvive by Juvederm

Allergan

This is the Skinvive by Juvederm identity captured in the dated Aesthetic Pass operational catalogue snapshot. Product-specific source verification is available at family level only.

Evidence status: Catalogue identity · family sources available

The clinical research edition

Go deeper into the formulation and evidence

Explore composition, mechanism, safety and study interpretations for the exact presentation below. These new clinical drafts have a separate review process; this identity profile’s approval does not extend to them.

Juvéderm Voluma XC monograph ↗

Identity record

What is recorded

v2026.08.15.1
Record type
Operational catalogue identity
Recorded maker
Allergan
Classification
Skin booster / biostimulator
Material identity
hyaluronic acid microdroplets
Snapshot date
14 August 2026

Manufacturer and category are catalogue fields. They are not, by themselves, a regulatory classification or verification of the exact marketed presentation.

Family evidence available

This identity maps to Juvéderm

The family profile provides aliases and official family-level sources. Those sources do not automatically verify this exact variant, formulation, label, or market status.

Open family profile

Provenance

Family-level sources

3 sources · checked 14 August 2026

These sources support the linked family profile, not every property of this exact catalogue identity.

  1. Manufacturer

    1. About the Juvéderm filler collection

    Allergan Aesthetics, an AbbVie company · United States

    Open source ↗

    Supports: Juvéderm family identity, named family context, and hyaluronic-acid material class.

  2. Regulator

    2. FDA-approved dermal fillers

    U.S. Food and Drug Administration · United States

    Open source ↗

    Supports: Regulatory-method context and the requirement to verify individual filler records and labels.

  3. Regulator

    3. JUVEDERM gel implants — PMA P050047

    U.S. Food and Drug Administration · United States

    Open source ↗

    Supports: The original US PMA family record, applicant identity, generic device class, and links to supplements and labeling.

Use boundary

What this record does not establish

  • Regulatory statusOnly within a source's named jurisdiction; family evidence does not establish status elsewhere.
  • Authenticity or supply chainA catalogue name cannot authenticate an individual box, lot, or seller.
  • Clinical suitabilityNo product selection, patient assessment, dose, protocol, or injection technique is provided.
  • Availability or equivalenceNames, formulations, units, and presentations can vary by market and over time.

Separate reference from record-keeping

Document the exact product and lot actually used

Aesthetic Pass records treatment identity, lot information, photos, and injection maps. The atlas itself never chooses a product or treatment.

Explore traceability