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On November 11, 2000, the U.S. Food and Drug Administration (FDA) issued an advisory concerning the safety of phenylpropanolamine (PPA). Wyeth Consumer Healthcare (formerly known as Whitehall-Robins) 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 HCl 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® Cold & Allergy Elixir Dimetapp® Cold & Allergy Elixir (lists pseudoephedrine HCl in the "active ingredients" section)
Dimetapp® DM Cold & Cough Elixir Dimetapp® DM Cold & Cough Elixir (lists pseudoephedrine HCl in the "active ingredients" section)
Dimetapp® 12-Hour Extentabs Dimetapp® 12-Hour Non-Drowsy Extentabs (lists pseudoephedrine HCl in the "active ingredients" section)
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 HCl in the "active ingredients" section)