LATISSE® eyelash enhancer is the first and only U.S. Food and Drug Administration-approved cosmetic treatment for increasing the length, thickness and darkness of eyelashes. Available only through prescription, it is applied once a day to the base of the upper eyelashes.
Latisse® is an FDA-approved treatment for the growth of eyelashes in patients with thin or missing eyelashes. It increases the length, thickness, and darkness of lashes. It is a liquid medication that is applied directly to the base of the eyelashes once a day. Results are usually apparent after 4-6 weeks and are frequently dramatic. Treatment should be continued for continued eyelash growth.
Latisse® should only be used under the care of an ophthalmologist, as the product can cause changes in eye pressure, darkening of the skin or iris (which can be permanent), or red and irritated skin. Although these problems are not common, our doctors can examine any ocular side effects to determine if your treatment can continue.
If you are interested in learning more about Latisse®, schedule a consultation with any of our doctors. Latisse® is available only by prescription but can be purchased directly through our office.
LATISSE® solution is applied at night. Contact lenses and makeup are removed, and skincare products applied, before using the LATISSE solution.To prevent contamination, the LATISSE® solution is applied with a single-use disposable applicator. The applicator, which is coated with one drop of solution, is applied to the base of the upper eyelid, at the lash line. The applicator is moved from the inside of the lash line to the outside. Excess solution is blotted to prevent its spreading to other areas. A separate applicator is used for each eye.
Contact lenses can be put back in 15 minutes after LATISSE® treatment.
Anyone who wants longer, fuller and darker eyelashes may be a candidate for LATISSE® treatment. Those who have eye infections, or broken or irritated skin on their eyelids, or who use products for elevated intraocular pressure, should not undergo LATISSE® treatment. A doctor-performed full medical history is taken prior to the start of LATISSE® treatment.
The common side effects of LATISSE® treatment end when treatment ends. Side effects include the following:
There is one potential serious side effect of treatment. According to the manufacturer’s website, LATISSE® treatment “may cause increased brown iris pigmentation of the colored part of the eye which is likely to be permanent,” although its occurrence is “very infrequent.”
Contact us to learn more about our Custom Latisse® procedure »
8025 Roosevelt Blvd.
Philadelphia, PA 19152
