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	© 2002 Wyeth  Consumer Healthcare  Privacy  Terms & Conditions	On November 11, 2000, the U.S. Food and Drug Administration (FDA) issued an advisory concerning the safety of phenylpropanolamine (PPA). Wyeth Consumer Healthcare immediately stopped shipping all PPA-containing products, removed these products from store shelves and began shipping reformulated products without PPA. Please find below a list of Wyeth Consumer Healthcare products that formerly contained PPA. To find out if a product in your medicine cabinet has PPA, check for phenylpropanolamine (PPA) in the "active ingredients" section. Products reformulated without PPA list pseudoephedrine in the "active ingredients" section. If you have a Dimetapp or Robitussin product that contains PPA, please discontinue use and call the following toll-free number for an exchange or refund: 1-800-762-4675, Monday-Friday 9 a.m. to 5 p.m. EST Products with PPA (discontinued November 2000) Products Formulated without PPA Dimetapp Elixir Dimetapp Elixir (Flagged "New Formula. Read directions carefully.") Dimetapp DM Dimetapp DM Dimetapp DM (Flagged "New Formula. Read directions carefully.") Dimetapp 12-Hour Extentabs Dimetapp 12-Hour Non-Drowsy Extentabs (Flagged "New". "Non-Drowsy" is in product name.) Dimetapp Cold & Allergy Chewable Tablets - Dimetapp 4-Hour Tablets - Dimetapp 4-Hour Liquigels - Dimetapp Cough & Cold Liquigels - Dimetapp Cold & Allergy Quick Dissolve Tablets - Robitussin CF Robitussin CF (lists pseudoephedrine in the “active ingredients” section)