RESTYLANE® Original with Lidocaine [European Edition]

RESTYLANE® Original with Lidocaine [European Edition] – 1mL × 1 Syringe | Galderma, Sweden

RESTYLANE® Original with Lidocaine is the classic NASHA-based hyaluronic acid filler from Galderma, ideal for correcting moderate facial wrinkles such as nasolabial folds and marionette lines. This European Edition includes 0.3% lidocaine for patient comfort, and is packaged in a 1mL pre-filled syringe for single-use injection into the mid-to-superficial dermis.

Field Name Example Value
Product Name RESTYLANE® Original with Lidocaine [European Edition] – 1mL × 1 Syringe
Product Code RES-EU-ORG-LD-1
Product Type Injectable Filler / Hyaluronic Acid
Category Dermal Filler / Wrinkle Correction / Mid-to-Superficial Dermis
Manufacturer Galderma Sweden AB
Appearance Transparent HA gel in sterile pre-filled syringe with luer-lock tip
Dosage / Units 1mL per syringe
Purity NASHA™ technology hyaluronic acid (non-animal stabilized) + 0.3% lidocaine
Quantity Options 1 syringe per box
Storage Store at 2–25°C; do not freeze; keep away from direct light
Shelf Life 24 months unopened
Packaging CE-certified European Galderma packaging with traceable serial and multilingual instruction leaflet
Manufacturer Origin Sweden
Use Classification Export Only – For professional clinical use; not for direct-to-consumer sales
Tags restylane original, galderma, hyaluronic acid filler, nasolabial folds, fine lines, lidocaine, EU version, BLUEBIOTECH

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

RESTYLANE® Original with Lidocaine – Versatile Dermal Filler for Fine Lines & Facial Contouring | Galderma, Sweden

Product Overview

RESTYLANE® Original with Lidocaine is a classic, non-animal stabilized hyaluronic acid (NASHA™) dermal filler developed by Galderma (Q-Med AB, Sweden). It is specially formulated to smooth moderate facial wrinkles, enhance contours, and restore natural volume with precision and safety.

With the addition of 0.3% lidocaine, this version offers increased comfort during injection, making it an excellent choice for treating nasolabial folds, marionette lines, tear troughs, and lip border definition. RESTYLANE® Original is considered the benchmark filler in the industry — clinically proven, globally trusted, and CE-certified.


Key Features & Benefits

  • NASHA™ Technology
    Unique cross-linked HA structure for precise placement and natural lift.

  • Lidocaine for Patient Comfort
    Minimizes pain during treatment without compromising viscosity or stability.

  • Versatile Applications
    Ideal for fine-to-moderate wrinkle correction, tear trough rejuvenation, and subtle contouring.

  • Swedish-Made Quality
    Produced by Galderma under EU GMP, with over 50 million treatments worldwide.

  • Reliable Longevity
    Results typically last 6 to 9 months, depending on injection area and technique.


Product Specifications

  • Product Name: RESTYLANE® Original with Lidocaine

  • Active Ingredient: Stabilized hyaluronic acid (20 mg/mL)

  • Lidocaine: 0.3%

  • Form: Injectable transparent gel

  • Syringe Volume: 1mL prefilled syringe

  • Needles: 2 × 29G

  • Injection Depth: Mid-to-deep dermis

  • Manufacturer: Galderma / Q-Med AB (Sweden)

  • Storage: 2–25°C

  • Shelf Life: 24 months from manufacturing


Recommended Indications

  • Nasolabial folds

  • Marionette lines

  • Perioral lines (smoker’s lines)

  • Tear troughs

  • Lip contour enhancement

  • Chin and cheek refinement (mild enhancement)


How It Works

RESTYLANE® Original is injected into the mid to deep dermis, where it integrates seamlessly into the surrounding tissue and provides support, hydration, and volume. Its firm NASHA™ gel texture allows for excellent shape retention while maintaining natural facial dynamics. The added lidocaine ensures a more comfortable experience with reduced post-treatment sensitivity.

For best results, Galderma recommends treatment by a certified injector and follow-up maintenance every 6–9 months depending on patient response.

Further reading:
Galderma RESTYLANE Official Website


Compliance Statement

This product is manufactured in Sweden by Galderma and is CE-certified for use by trained medical professionals. It is intended strictly for aesthetic medical procedures and must be administered by licensed practitioners. Not for retail sale, over-the-counter purchase, or at-home use. Importers are responsible for compliance with local regulations and medical device laws.


Tags / Keywords

Restylane Original, Galderma Dermal Filler, Swedish Hyaluronic Acid, Mid Dermis Filler, Lip Contour Filler, Tear Trough Filler, Wrinkle Correction Injection, HA Filler with Lidocaine, CE Certified Filler, Non-Animal HA Gel

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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