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  2. 8 Lots of This Popular Cough Syrup Have Been Recalled ... - AOL

    www.aol.com/8-lots-popular-cough-syrup-202500662...

    Haleon, maker of Robitussin cough medicine, has announced a recall of certain Robitussin cough syrups due to a possible microbial contamination that could lead to deadly infections for at-risk ...

  3. Haleon to recall batches of some adult cough syrups due to ...

    www.aol.com/news/haleon-recall-batches-adult...

    The consumer healthcare company is recalling the cough syrup, sold under the brand name "Robitussin Honey CF Max Day Adult" in 4-ounce and 8-ounce doses, along with its 8-ounce night-time version.

  4. Benadryl - Wikipedia

    en.wikipedia.org/wiki/Benadryl

    Benadryl Dry, Tickly Cough Liquid is a cough medicine found in Australia. It is used to temporarily relieve irritating coughs. Pholcodine is the main ingredient found in this cough liquid. [11] This medication is to be taken orally and may cause drowsiness. In India, Benadryl can also be found in the form of a cough liquid and also cough lozenges.

  5. Robitussin Is Recalling Cough Medicine Due To Microbial ... - AOL

    www.aol.com/robitussin-recalling-cough-medicine...

    As for Robitussin Honey CF Max Day Adult (8 oz), lot numbers include T08730, T08731, T08732, and T08733 with the expiration date of May 31, 2025, and T10808 with the expiration date of September ...

  6. Habit cough - Wikipedia

    en.wikipedia.org/wiki/Habit_cough

    Habit cough is commonly characterized by a harsh barking cough, and can persist for weeks, months, and even years. The cough's hallmarks are severe frequency, sometimes a cough every 2–3 seconds, and the lack of other symptoms such as fever. The patient can have trouble falling asleep but once asleep will not cough.

  7. Dextromethorphan - Wikipedia

    en.wikipedia.org/wiki/Dextromethorphan

    Dextromethorphan, sold under the brand name Robitussin among others, is a cough suppressant used in many cough and cold medicines. [6] In 2022, the US Food and Drug Administration (FDA) approved the combination dextromethorphan/bupropion to serve as a rapid-acting antidepressant in people with major depressive disorder.

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