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Dextromethorphan (DXM), sold under the trade 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 patients with major depressive disorder .
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 ...
Robitussin Honey CF Max Day and Nighttime are cough syrups indicted for the temporary relief of symptoms occurring with cold or flu, hay fever, or other respiratory allergies, according to Haleon.
Alaska House Bill No. 125 [2] placed regulations on who can sell and who can buy products that contain any level of dextromethorphan. The provider must check the identification of a person wishing to purchase dextromethorphan-containing products to verify that the purchaser is 18 years of age or older.
The maker of Robitussin cough syrup is recalling several lots of products containing honey due to contamination that could pose a serious risk to people with weakened immune systems. Haleon’s ...
Cough medicine containing dextromethorphan in tablet form (15mg) Dextromethorphan, or DXM, a common active ingredient found in many over-the-counter cough suppressant cold medicines, is used as a recreational drug and entheogen for its dissociative effects. [1]
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