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  2. Tylenol (brand) - Wikipedia

    en.wikipedia.org/wiki/Tylenol_(brand)

    On January 15, 2010, a voluntary recall of several hundred batches of popular medicines was announced, including Benadryl, Motrin, Rolaids, Simply Sleep, St. Joseph Aspirin, and Tylenol. [16] The recall was due to complaints of a musty smell suspected to be due to contamination of the packaging with the chemical 2,4,6-tribromoanisole. [17]

  3. Kids over-the-counter medicine recalled for problem that can ...

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  4. Tylenol, Motrin, Benadryl recalls spur criminal probe ...

    www.aol.com/news/2010-05-27-tylenol-motrin...

    Top Food and Drug Administration officials told a congressional committee today that Johnson & Johnson, the venerable manufacturer of Children's Tylenol, Motrin, Benadryl and other children's ...

  5. Not just Tylenol and Motrin: Drug recalls skyrocketing

    www.aol.com/news/2010-08-17-not-just-tylenol-and...

    Recalls of Tylenol, Motrin and Benadryl might have received the most attention, but they were just part of the story as recalls of over-the-counter (OTC) and prescription drugs quadrupled in 2009 ...

  6. Lawsuits claiming Tylenol causes autism lack scientific ...

    www.aol.com/news/lawsuits-claiming-tylenol...

    December 19, 2023 at 3:57 PM. By Brendan Pierson ... The lawsuits also targeted retailers that sold their own generic versions of Tylenol, including CVS, Walgreens and Walmart. CVS and Walgreens ...

  7. Excedrin (brand) - Wikipedia

    en.wikipedia.org/wiki/Excedrin_(brand)

    Contains 250 mg acetaminophen, 250 mg aspirin and 65 mg caffeine. 1969: Excedrin PM – Excedrin PM is the first headache and sleeping pill combination product. [8] Contains 500 mg acetaminophen and 38 mg diphenhydramine citrate as a sleep aid. Those same active ingredients were later utilized several years later in the product Tylenol PM.

  8. Parents call out Children's Tylenol price gouging amid ...

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  9. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]