Restylane Eyelight is indicated for the improvement of infraorbital hollowing in patients over the age of 21.

As you age, your facial skin begins to lose its elasticity and volume. As a result, the face droops and shifts downwards, and your facial features may appear as hollow, such as the area under your eyes. Restylane® Eyelight injectable gel is designed to temporarily restore volume to the hollows under the eyes in patients over the age of 21. Restylane® Eyelight is intended for patients that are beginning to see a hollow appearance under the eyes. Restylane® Eyelight has been shown to maintain this effect for up to 12 months.

Restylane Eyelight is a transparent, viscous, and sterile gel of hyaluronic acid (HA) generated by Streptococcus species of bacteria, chemically crosslinked with BDDE (1.4-butanediol diglycidyl ether). The gel is suspended in phosphate buffered saline pH 7 at a HA concentration of 20 mg/mL with 0.3% lidocaine.

Contraindications

• Restylane Eyelight is contraindicated for patients with severe allergies manifested by a history of anaphylaxis or history or presence of multiple severe allergies.
• Restylane Eyelight contains trace amounts of gram-positive bacterial proteins and is contraindicated for patients with a history of allergies to such material.
• Restylane Eyelight contains lidocaine and is contraindicated for patients with a history of allergies to such material or other amide type anesthetics.

After-care

• Avoid touching the treated area within six hours following treatment so you do not accidentally injure your skin while the area is numb. After that, the area can be gently washed with soap and water.
• For the first 24 hours, you should avoid or minimize hard (strenuous) exercise. You should also avoid or minimize exposure to extensive sun or extreme temperatures. Exposure to any of these may cause the area where you were treated to temporarily become red, swell and/or itch. If you experience any of these, an ice pack can be applied for relief.
• Avoid taking aspirin, NSAID, blood thinners, and high doses of Vitamin E supplements for one week after treatment. These agents may increase bruising and bleeding at the injection site.