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That said, immunocompromised people who used Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult cough syrups from the recalled lots may be at risk of fungemia (fungi or ...
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.
Robitussin Honey CF Max NT Adult 8oz Lots: T08740 (June 30, 2026), T08742 (June 30, 2026) The elderly and very young people are most likely to experience complications from fungemia.
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 .
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 ...
Dextromethorphan is a cough suppressant found in several cold medications. Several U.S. states have begun regulating who, and under what circumstances, can purchase dextromethorphan containing products. Not all states have regulations documented at this time, but this article contains all the states that have documentation.
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