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FDA: Procter & Gamble Unlawfully Marketing Two Vicks Cold and Flu Medicines Containing Vitamin C

30 October 2009 2,041 views No Comment

FDA: Procter & Gamble Unlawfully Marketing Two Vicks Cold and Flu Medicines
Containing Vitamin C

SILVER SPRING, Md., Oct. 30 /PRNewswire-USNewswire/ — The U.S. Food and Drug
Administration today sent a warning letter to Procter & Gamble notifying the
company that its Vicks DayQuil Plus Vitamin C and Vicks Nyquil Plus Vitamin C
are illegally marketed combinations of drug ingredients and a dietary

(Logo:  http://www.newscom.com/cgi-bin/prnh/20090824/FDALOGO )

Both of the over-the-counter (OTC) medicines, which contain vitamin C in
addition to several drug ingredients, are marketed as treatments for cold and
flu symptoms. The FDA took the action against the Cincinnati-based company:

    —  To clarify that these single dosage form combinations of drug
        ingredients and dietary ingredients legally cannot be marketed because
        they have not been proven safe and effective, and

    —  Because the agency previously determined that there are insufficient
        data to show that vitamin C is safe and effective in preventing or
        treating the common cold.
Under its OTC monograph system, the FDA allows some OTC drugs to be marketed
without agency approval. Such drugs must comply with applicable monographs,
which are regulations that set requirements for the drugs’ labeling,
formulations and indications. The two Vicks products do not comply with the
applicable FDA monograph and must first be evaluated and approved under the
FDA’s new drug approval process to be legally marketed.

The FDA’s position on the regulatory status of OTC drug products that combine
drug ingredients with dietary ingredients in a single dosage form has been
described in previous warning letters issued in 2001 and 2008. The agency’s
position on the marketing of vitamin C for preventing or treating the common
cold also has been stated in a number of previous warning letters.

(Editor’s note: The warning letter sent to Procter & Gamble today concerns the
same products as the letter mistakenly posted on the FDA Web site on Oct. 14,
2009, due to a computer error.)

For more information

FDA Warning Letter to Procter & Gamble

FDA Drug Safety Initiative http://www.fda.gov/cder/drugSafety.htm

Media Inquiries: Christopher Kelly, 301-796-4676,
Consumer Inquiries: 888-INFO-FDA

SOURCE  U.S. Food and Drug Administration

Media Inquiries: Christopher Kelly of FDA, +1-301-796-4676,
© Thomson Reuters 2009 All rights reserved

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