BELOTERO® BALANCE with Lidocaine

Key features of BELOTERO® BALANCE with Lidocaine include:

• Cross-linked sodium hyaluronate: 22.5 mg/mL
• Lidocaine hydrochloride: 3.0 mg/mL
• Gel presentation: Pre-filled glass syringe with two sterile needles
• Viscoelastic properties: Bioresorbable and non-pyrogenic
• Indication: Intended for the correction of moderate to severe facial wrinkles and folds, particularly nasolabial folds
• Sterility: Packaging ensures the product remains sterile until use

Indications for BELOTERO® BALANCE with Lidocaine include the correction of moderate to severe facial wrinkles and folds. It is especially effective for nasolabial folds, enhancing facial aesthetics with smooth results.

• Contraindications include a known hypersensitivity to lidocaine or other ingredients, severe allergies, or a history of anaphylactic reactions.
• Precautions: BELOTERO® BALANCE should not be injected into blood vessels. Care must be taken to avoid intravascular injections, as these can lead to vascular occlusion, necrosis, or more severe complications like blindness.
• Side Effects: Common side effects include swelling, bruising, pain, redness, and induration at the injection site. These reactions are typically mild to moderate and subside within a few days.

BELOTERO® BALANCE with Lidocaine contains the following key components:

• Sodium Hyaluronate (22.5 mg/mL): A naturally occurring substance that helps to provide volume and hydration to the skin.
• Lidocaine (3.0 mg/mL): A local anesthetic used to minimize pain during the injection process.
• Buffer: A physiological buffer at pH 7.
• Packaging: The product is supplied in a pre-filled glass syringe, which contains 1 mL of gel and is packaged with two sterile needles. The product is designed for single-use only and should not be re-sterilized.
• Storage: BELOTERO® BALANCE should be stored at room temperature (up to 25°C) and must not be frozen.

BELOTERO® BALANCE with Lidocaine should only be administered by a qualified healthcare professional with appropriate training. The product is injected into the mid-to-deep dermis of the skin, typically for the correction of nasolabial folds.

• Preparation: The syringe should be prepared by attaching the provided sterile needle securely.
• Injection: The gel is injected using gentle pressure to ensure even distribution. The typical volume injected is approximately 1.59 mL for each nasolabial fold, depending on the degree of correction needed.
• Techniques: Injection techniques may include linear threading, serial puncture, or fanning.
• Post-Treatment Care: After treatment, patients should avoid touching or pressing on the treated areas for 12-24 hours. They should also avoid excessive sun exposure, alcohol, or strenuous physical activity for up to 24 hours post-treatment.

By following these guidelines, BELOTERO® BALANCE provides a safe and effective solution for facial wrinkle treatment with enhanced patient comfort due to the inclusion of lidocaine