Belotero® Soft With Lidocaine (1 x 1ml)

General Information

BELOTERO® Soft with Lidocaine is an injectable hyaluronic acid-based dermal filler developed by Merz Aesthetics. It contains 20 mg/mL of cross-linked sodium hyaluronate and 0.3% lidocaine (3 mg/mL) to help reduce discomfort during injection. Its soft gel formulation is designed to correct fine lines and superficial facial wrinkles while supporting a smooth, natural-looking appearance.

The product is supplied in a prefilled 1 mL syringe and is intended for administration by appropriately trained healthcare professionals in accordance with the manufacturer’s instructions and applicable local regulations.

Indications for BELOTERO® Soft with Lidocaine

BELOTERO® Soft is designed to improve the appearance of fine lines and shallow facial wrinkles.

Potential treatment objectives include:

• Perioral wrinkle correction: Helps soften fine lines around the mouth.
• Fine line smoothing: Improves the appearance of superficial facial wrinkles.
• Skin texture refinement: Supports a smoother-looking skin surface.
• Shallow depression correction: Helps correct selected superficial facial depressions, depending on the applicable product labeling.
• Natural-looking results: Provides subtle correction while maintaining natural facial expressions.

The product is intended for injection into the superficial to mid-dermis. 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: Hypersensitivity to sodium hyaluronate, lidocaine, or other product components.
• Pregnancy and breastfeeding: Treatment is contraindicated under the cited product instructions.
• Age restrictions: Not intended for individuals under 18 years of age.
• Active infections: Treatment should be avoided in patients with a general infection or active infection or inflammation at the treatment site.
• Autoimmune conditions: Active autoimmune disease is a contraindication under the cited instructions.

Potential Side Effects

Common side effects include redness, swelling, bruising, tenderness, itching, pain, and temporary lumps at the injection site. These reactions are generally mild to moderate and often resolve within a few days.

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 require immediate emergency medical attention.

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