FDA approves Allergan’s Latisse

January 6, 2009

Irvine, Calif. - The Food and Drug Administration (FDA) has approved Latisse (bimatoprost ophthalmic solution)0.03 percent for the treatment of eyelash hypotrichosis, according to Allergan.

Irvine, Calif.

- The Food and Drug Administration (FDA) has approved Latisse (bimatoprost ophthalmic solution)0.03 percent for the treatment of eyelash hypotrichosis, according to Allergan.

Latisse will be the only FDA approved treatment to improve eyelash length, darkness and thickness, according to a press release.

Latisse will be available within the first quarter of 2009.

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