Allergan Receives FDA Warning Letter re Latisse Eyelash Thickener

The Food and Drug Administration sent a warning letter to Allergan concerning its eyelash thickener Latisse. In the letter dated Sept. 10 and posted to the FDA Web site on Sept. 17, the FDA states that the Latisse Web site does not include adequate warnings for possible side effects from using Latisse, and asks the company to comply with its request to modify the site. Allergan must reply to the letter by Sept. 24.

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