$93.00 – $870.00Price range: $93.00 through $870.00
Brand: Restylane® Eyelight with Lidocaine (0.5 ml)
Manufacturer: Galderma
Active Substance(s): Hyaluronic acid, lidocaine
Strength: 20 mg/ml HA, 3 mg/ml lidocaine
Pack Size: 1 x 0.5 ml pre-filled syringe
General Information
Restylane® Eyelight with Lidocaine is a hyaluronic acid-based injectable dermal filler 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 restore volume in hollow areas beneath the eyes, helping create a smoother, refreshed appearance.
The product is supplied in a 0.5 mL prefilled 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® Eyelight with Lidocaine
Restylane® Eyelight is specifically designed to improve the appearance of under-eye hollows.
Potential treatment objectives include:
- Under-eye hollow correction: Helps restore volume in depressed areas beneath the eyes.
- Tear trough treatment: Softens the appearance of hollowing between the lower eyelid and cheek.
- Reduced tired appearance: Helps create a fresher, more rested look.
- Facial rejuvenation: Improves under-eye contours for a smoother appearance.
- Natural-looking results: Supports subtle volume restoration when appropriately selected and administered.
In the United States, Restylane® Eyelight is indicated to improve infraorbital hollowing in adults aged 21 and older. Approved indications may vary by country.
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:
- Severe allergies: A history of anaphylaxis or multiple severe allergies.
- Ingredient sensitivities: Allergy to lidocaine, other amide-type local anesthetics, or relevant bacterial proteins.
- Bleeding disorders: Patients with bleeding disorders should not receive treatment where contraindicated by the product instructions.
- Active skin conditions: Treatment should be avoided in areas with active infection or inflammation.
- Pregnancy and breastfeeding: Safety has not been established.
Potential Side Effects
Common side effects include swelling, redness, bruising, tenderness, pain, itching, and temporary lumps around 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 require immediate emergency medical attention.
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