Description

JUVÉDERM VOLUMA with Lidocaine is a sterile, cross-linked hyaluronic acid injectable gel implant manufactured by Allergan. It is intended for professional restoration of facial volume, subject to the authorised indications and regulations in the country where it is used.

Each 1 ml syringe contains 20 mg of hyaluronic acid gel and 3 mg of lidocaine hydrochloride. A standard box contains two 1 ml prefilled syringes and four sterile, single-use 27G ½-inch needles.

What is JUVÉDERM VOLUMA?

JUVÉDERM VOLUMA is a professional facial filler within the JUVÉDERM collection. The product is a sterile, clear, colourless and physiological gel made with cross-linked hyaluronic acid of non-animal origin.

The official instructions describe JUVÉDERM VOLUMA as an injectable implant intended to restore facial volume. The presence of lidocaine is intended to help reduce the patient’s pain during professional administration.

Authorised applications may vary between countries. Practitioners must consult the instructions included with the actual product and follow the regulations applying in their location.

JUVÉDERM VOLUMA product specifications

• Product name: JUVÉDERM VOLUMA with Lidocaine
• Product type: Cross-linked hyaluronic acid injectable gel implant
• Hyaluronic acid: 20 mg per 1 ml syringe
• Lidocaine hydrochloride: 3 mg per 1 ml syringe
• Lidocaine concentration: 0.3%
• Individual syringe volume: 1 ml
• Pack size: Two prefilled syringes
• Total gel volume: 2 ml
• Needles included: Four sterile 27G ½-inch single-use needles
• Manufacturer: Allergan
• Manufacturing location: France
• Storage conditions: 2–25°C
• Intended user: Authorised and appropriately qualified medical practitioners

Key features of JUVÉDERM VOLUMA

JUVÉDERM VOLUMA contains a structured cross-linked hyaluronic acid gel intended to restore temporary physical volume within the face. Its formulation is distinct from softer JUVÉDERM products intended for fine lines or lip-related applications.

The gel is presented in graduated, prefilled, disposable syringes. Each standard pack also includes sterile needles, an instruction leaflet and labels intended to support product and patient traceability.

The product contains lidocaine at 0.3%. Lidocaine is a local anaesthetic included to improve comfort during administration, but it does not eliminate all discomfort or procedural risk.

Hyaluronic acid and lidocaine

Hyaluronic acid: Each syringe contains 20 mg of cross-linked hyaluronic acid gel. Hyaluronic acid is used in absorbable filler products to provide temporary volume and physical tissue support.

Lidocaine hydrochloride: Each syringe contains 3 mg of lidocaine hydrochloride. Patients must disclose any previous allergy or sensitivity to lidocaine or other amide local anaesthetics.

The complete formulation also contains a phosphate buffer adjusted to pH 7.2. Healthcare professionals must read the enclosed instructions for complete composition, contraindications, warnings and precautions.

JUVÉDERM VOLUMA compared with VOLUX

VOLUMA and VOLUX are different products within the JUVÉDERM collection. Their names, compositions and authorised purposes should not be treated as interchangeable.

• JUVÉDERM VOLUMA: Contains 20 mg hyaluronic acid gel per 1 ml syringe and is intended to restore facial volume.
• JUVÉDERM VOLUX: Contains 25 mg hyaluronic acid gel per 1 ml syringe and is intended to restore and create facial volume, with more specific chin and jaw indications in certain markets.

Both products contain 3 mg of lidocaine hydrochloride per 1 ml syringe. The appropriate formulation must be selected by the treating medical practitioner following an individual assessment.

Professional consultation and assessment

JUVÉDERM VOLUMA must only be administered by an authorised medical practitioner with appropriate anatomical knowledge, training, insurance and legal authority. It must not be self-injected or administered at home.

A professional consultation should review the patient’s medical history, allergies, current medication, previous fillers, existing implants, skin condition and treatment expectations.

The official instructions identify contraindications and precautions that must be considered. These include known sensitivity to hyaluronic acid, lidocaine, amide local anaesthetics or relevant bacterial proteins.

Potential risks, complications, alternatives and aftercare should be explained before treatment. Individual results can vary, and no exact outcome or duration should be guaranteed.

Areas excluded by the instructions

The official product instructions state that JUVÉDERM VOLUMA should not be injected into the periorbital area, glabellar region, lips or blood vessels. It should not be used to overcorrect a treatment area.

This information is provided as a safety summary, not as an administration guide. The complete instructions supplied by Allergan must be read and followed by the treating practitioner.

Packaging and authenticity checks

Inspect the JUVÉDERM VOLUMA box before professional use. Confirm the manufacturer details, two-syringe presentation, ingredient information, batch number, expiry date, seals and traceability labels.

Do not use the product if the box, sterile packaging, syringe or needle packaging is damaged, opened or altered. Products whose authenticity or storage history cannot be established should not be administered.

Retain the invoice, original packaging, batch details and patient traceability labels. These records may be required if a product complaint or safety incident needs to be investigated.

Storage and responsible handling

Store JUVÉDERM VOLUMA between 2°C and 25°C in accordance with the manufacturer’s instructions. Keep the product in its original packaging and protect it from unsuitable temperatures and unauthorised access.

Each syringe and needle is intended for single-patient use. Used, open, damaged or expired products must be disposed of according to applicable infection-control, sharps and clinical-waste procedures.

Important regulatory information

This page contains general commercial product information. It is not medical advice, an injection protocol or confirmation that every international indication applies within the United Kingdom.

Purchasers are responsible for verifying the product’s authenticity, conformity marking, regulatory status and permitted use. Professionals must read and follow the instructions included with the specific box.

For complete manufacturer information, review the official JUVÉDERM VOLUMA instructions for use. You can also browse other professional products from The Clinic Vault shop.

Order JUVÉDERM VOLUMA

A standard box contains two 1 ml prefilled syringes and four sterile 27G ½-inch needles. Before ordering, confirm that the packaging, regional version, expiry date and conformity information meet your professional requirements.

Add JUVÉDERM VOLUMA to your basket when ready, or contact The Clinic Vault for clarification about availability or packaging. This medical device is supplied for authorised professional use and must not be self-administered.