LATISSE®
GET NATURAL LONG AND FULLER LASHES AS SOON AS 8 WEEKS!**
(FDA APPROVED)
Results were proven in our clinical study.
The LATISSE® clinical study was conducted at 16 sites across the country and included 278 participants of varying ages between 22 & 78. The study tested LATISSE® solution and a placebo (LATISEE® without its active ingredient that stimulates and darkens lashes). Neither patients nor clinical investigators knew which group received what treatment. By week 16, the results showed that 78% (107/137) of participants experienced a significant increase in overall eyelash prominence (including elements of length, fullness and darkness), compared to 18% (26/141) for the placebo group.**
CLINICAL TRIAL RESULTS SHOWED LASHES WERE:**
- 25% LONGER (2% for placebo)
- 106% FULLER (12% for placebo)
- 18% DARKER (3% for placebo)
SIDE EFFECTS ARE POSSIBLE. HERE’S WHAT TO LOOK OUT FOR.
Latisse may produce some side effects, the most common of which are itching sensations in the eyes and/or redness. This side effect was reported in approximately 4% of patients.
Other less common side effects typically occur on the skin close to where LATISSE® is applied or in the eyes.
If you are using LATISSE® solution and you develop a new ocular condition or reaction (e.g., trauma or infection) or experience a sudden decrease in visual acuity be sure to talk to your doctor immediately concerning the continued use of LATISSE®.
For more information or to set up an appointment please contact us at (480) 781 -0744.
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