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MultiVu Video Feed: U.S Food and Drug Administration (Fda) Approves Latisse(TM) --
Date:12/26/2008

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NEWS: U.S Food and Drug Administration (FDA) Approves LATISSE(TM) -- First and Only FDA Approved Treatment to Enhance Eyelash Prominence, including Length, Thickness and Darkness.

FORMAT: B-roll and Soundbites

ADDITIONAL RESOURCES: Video, contact information and more available at: http://www.prnewswire.com/broadcast/36437/press.html


    SOUNDBITES:
    * Frederick Beddingfield, III, MD, PhD, Chief Medical Officer for
      Allergan Medical and Vice President and Therapeutic Area Head for
      Dermatology Clinical Research and Development at Allergan
    * Doris Day, MD, LATISSE(TM) Clinical Investigator
    * Cindy Ross, LATISSE(TM) Clinical Trial Patient
    * Diane Diamondstein, LATISSE(TM) Clinical Trial Patient

    B-ROLL INCLUDES:
    * Close-up of eyes and eyelashes
    * Photo of patient applying LATISSE(TM)
    * Patient before and after photos

VIDEO PROVIDED BY: Allergan, Inc.

Contact: FOR MORE INFORMATION, PLEASE CALL: MultiVu Media Relations, 1-800-653-5313 EXT. 3


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SOURCE Allergan, Inc.
Copyright©2008 PR Newswire.
All rights reserved

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