Restylane Skinbooster Vital With Lidocaine (1x1ml)

General Information

Restylane® Skinboosters Vital with Lidocaine is an injectable skin-conditioning product developed by Galderma. It contains 20 mg/mL of stabilized hyaluronic acid and 0.3% lidocaine (3 mg/mL) to help reduce discomfort during injection. Its formulation is designed to improve skin hydration, elasticity, smoothness, and overall skin quality.

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 Restylane® Skinboosters Vital with Lidocaine

Restylane® Skinboosters Vital is designed to improve skin quality and hydration in suitable treatment areas.

Potential treatment objectives include:

• Skin hydration: Helps improve moisture retention through the water-binding properties of hyaluronic acid.
• Improved elasticity: Supports skin flexibility and a smoother appearance.
• Skin texture: Helps improve skin smoothness and overall quality.
• Facial rejuvenation: Supports a refreshed appearance by improving skin hydration and texture.
• Treatment of selected areas: May be used on the face, neck, décolletage, and hands, depending on the applicable product labeling and clinical assessment.

The product is injected into the dermis by a qualified healthcare professional. Approved indications may vary by country, so the manufacturer’s current instructions for use should be consulted.

Contraindications and Precautions

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

Important precautions include:

• Severe allergies: A history of serious allergic reactions requires careful assessment.
• Ingredient sensitivities: Hypersensitivity to hyaluronic acid fillers, lidocaine, or amide-type local anesthetics.
• Bacterial protein sensitivity: Relevant sensitivities should be assessed according to the manufacturer’s instructions.
• Bleeding risks: Bleeding disorders or anticoagulant use may increase bruising.
• Active skin infections: Treatment should be postponed until the affected area has healed.
• Pregnancy and breastfeeding: Safety has not been established.

Potential Side Effects

Common side effects include redness, swelling, bruising, tenderness, itching, pain, and temporary lumps at injection sites. These reactions are generally temporary.

Rare but serious complications include infection, 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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