JUVÉDERM® ULTRA 3 [European Edition]

JUVÉDERM® ULTRA 3 [European Edition] – 1mL × 2 Pre-Filled Syringes | Allergan, Ireland

JUVÉDERM® ULTRA 3 [European Edition] is a versatile HA-based dermal filler for the correction of moderate facial lines and volume loss. Its medium gel consistency allows for natural-looking enhancement of nasolabial folds, marionette lines, and lips. Each box includes two 1mL syringes with 0.3% lidocaine to reduce discomfort during injection. Manufactured in Ireland and CE-certified.

Field Name Example Value
Product Name JUVÉDERM® ULTRA 3 [European Edition] – 1mL × 2 Pre-Filled Syringes
Product Code JUV-EU-U3-2X1
Product Type Injectable Filler / Hyaluronic Acid
Category Dermal Filler / Moderate Wrinkle Correction / Lip & Nasolabial Volume
Manufacturer Allergan Pharmaceuticals Ireland
Appearance Clear, smooth HA gel in sterile pre-filled syringes
Dosage / Units 1mL per syringe × 2 syringes per box
Purity Hyaluronic acid 24 mg/mL + 0.3% lidocaine
Quantity Options 2 syringes per box
Storage Store at 2–25°C; avoid freezing and direct sunlight
Shelf Life 24 months unopened
Packaging CE-marked European packaging with multilingual insert and tamper-proof serialization
Manufacturer Origin Ireland
Use Classification Export Only – For licensed professional use; not for retail or direct-to-consumer sales
Tags juvederm ultra 3, hyaluronic acid filler, nasolabial folds, lip enhancement, CE certified, lidocaine, allergan, BLUEBIOTECH

⚠️This product is labeled for Research Use Only (RUO). Not for human or veterinary therapeutic use.
See RUO Declaration for more info.

JUVÉDERM® ULTRA 3 [European Edition] – Versatile HA Filler for Moderate Wrinkles & Lip Volume | Allergan, Ireland

Product Overview

JUVÉDERM® ULTRA 3 is a versatile hyaluronic acid dermal filler developed by Allergan (Ireland), engineered to treat moderate facial wrinkles and enhance lip volume with smooth, natural-looking results. As part of the European Edition portfolio, it is CE-certified for medical use across the EU and other regulated global markets.

Formulated with 24 mg/mL cross-linked HA and 0.3% lidocaine, JUVÉDERM® ULTRA 3 provides a balance of volume, elasticity, and comfort — ideal for midface correction and fuller lip augmentation.

Explore Allergan’s aesthetic solutions at Allergan Aesthetics.


Key Features & Benefits

  • Smooths Moderate Wrinkles & Folds
    Designed for nasolabial folds, marionette lines, and chin wrinkles.

  • Enhances Lip Volume & Contour
    Provides fuller lips with soft projection and precise shape definition.

  • With Lidocaine for Patient Comfort
    Contains 0.3% lidocaine to reduce discomfort during injection.

  • Soft, Long-Lasting Results
    Clinical duration typically ranges from 9 to 12 months.

  • CE-Certified | European Edition
    Manufactured in Ireland under strict EU-GMP standards.


Product Specifications

  • Product Name: JUVÉDERM® ULTRA 3 – European Edition

  • Active Ingredient: Hyaluronic Acid (24 mg/mL)

  • Lidocaine: 0.3%

  • Form: Cross-linked, smooth HA injectable gel

  • Packaging: 2 × 1.0 mL pre-filled syringes

  • Needles Included: 4 × 27G

  • Injection Depth: Mid to deep dermis

  • Manufacturer: Allergan, an AbbVie company (Ireland)

  • Shelf Life: 24 months

  • Storage: 2–25°C


Recommended Treatment Areas

  • Moderate nasolabial folds (smile lines)

  • Marionette lines

  • Chin and perioral wrinkles

  • Full lip augmentation and vermilion border definition

  • Facial zones requiring soft projection and volumizing


How It Works

JUVÉDERM® ULTRA 3 uses Hyalcross™ Technology, a proprietary cross-linking process that produces a smooth, cohesive HA gel with excellent spreadability and durability. It integrates into the dermis to fill wrinkles or add volume while maintaining natural facial movement.

The result is visible enhancement in treated areas with minimal swelling, immediate effect, and sustained aesthetic improvement for months. The integrated lidocaine allows for a more comfortable patient experience throughout the procedure.

For clinical data and application guidance, visit PubMed – Juvederm Ultra 3.


Compliance Statement

This product is manufactured in Ireland by Allergan (an AbbVie company) and complies with European CE medical device standards. It is intended for administration by licensed aesthetic medical professionals only. It must not be resold to unlicensed users or used for self-injection. All importers and providers are responsible for compliance with local regulations.


Tags / Keywords

Juvederm Ultra 3, Midface Filler, Nasolabial Fold Injection, CE Hyaluronic Acid Filler, HA Filler with Lidocaine, Allergan Lip Filler, Moderate Wrinkle Treatment, Lip Volume Injection, Ireland-Made Dermal Filler, Juvederm for Smile Lines

Corporate Advantages

High-Purity Standards

Tested for purity and identity. COAs available
for all RUO compounds

Buyer Protection

Protected and discrete fulfillment
available upon request

Research-Grade Support

Dedicated service for labs, clinics, and
compounders handling RUO items.

Lab-Grade Quality Assurance

All compounds are tested for-identity and purity, COAs and supporting documentation are available upon request.

Strict RUO Compliance

All products are labeled for Researd Use Only (RUO), Not intended for human or veterinary therapeutic or diagnostic purposes.

Lab-Grade Quality Assurance

Custom branding.
white-label optionons and formulation assistancee available for eligible research institutions and partners.

Custom R&D & APl Synthesis

We support original
pharmaceutica solutions.custom research projects, and NDC-grade materials-meeting speifica.tions for qualified partners.

Serving Professionals Across the U.S.& Mexico

Trusted by MedSpas, wellness clinics and licensed compounders under licensed compounding relationships.

Secure & Discreet Fulfillment

Cold-chain shipping : private, plain.wrap packaging, and tracking for sensitive RUO materials.

⚠️ All compounds are provided strictly for Research Use Only (RUO). BLUEBIOTECH does not endorse or support clinical, therapeutic, or diagnostic use of its products unless under licensed compounder supervision.

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