Belotero® Volume Lidocaine (2 x 1ml)

General Information

BELOTERO® Volume Lidocaine is an injectable hyaluronic acid-based dermal filler developed by Merz Aesthetics. It contains 26 mg/mL of cross-linked sodium hyaluronate and 0.3% lidocaine (3 mg/mL) to help reduce discomfort during injection. Its dense, elastic gel formulation is designed to restore facial volume, improve contours, and provide structural support for natural-looking rejuvenation.

The product is supplied in prefilled syringes, with packaging quantities varying by market. It is intended for administration by appropriately trained healthcare professionals in accordance with the manufacturer’s instructions and local regulations.

Indications for BELOTERO® Volume Lidocaine

BELOTERO® Volume Lidocaine is designed to restore facial volume and enhance definition in appropriate treatment areas.

Potential treatment objectives include:

• Cheek augmentation: Restores volume and improves cheek fullness.
• Temple rejuvenation: Helps address hollowing in the temple area.
• Chin enhancement: Improves chin projection and facial proportions.
• Deep wrinkle correction: Helps soften severe nasolabial folds extending from the nose toward the corners of the mouth.
• Facial contouring: Supports balanced facial proportions and a rejuvenated appearance.

The product is intended for injection into deep facial tissue layers. Approved indications may vary by country, so consult the manufacturer’s current instructions for use.

Contraindications and Precautions

Before treatment, a qualified practitioner should review the patient’s medical history, allergies, medications, and previous aesthetic procedures.

Important contraindications and precautions include:

• Ingredient allergies: Known hypersensitivity to sodium hyaluronate, lidocaine, or other product components.
• Pregnancy and breastfeeding: Treatment is contraindicated under applicable product instructions.
• Age restrictions: Not intended for individuals under 18 years of age.
• Active infections: Treatment should be postponed in patients with general infections or active infections affecting the treatment area.
• Autoimmune conditions: Active autoimmune disease may contraindicate treatment under the applicable product labeling.

Always consult the current manufacturer’s instructions before treatment.

Potential Side Effects

Common side effects include redness, swelling, bruising, tenderness, pain, itching, and temporary lumps at the injection site.

Rare but serious complications include vascular occlusion, tissue necrosis, visual impairment, blindness, and stroke. Severe pain, unusual skin discoloration, sudden visual changes, or neurological symptoms following injection require immediate emergency medical attention.

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