The U.S. Food and Drug Administration (FDA) announced today that it is proposing a new rule to stop the use of an ingredient ...

The Food and Drug Administration (FDA) is proposing to remove from the ... with others to ease cold and flu symptoms in ...

The Food and Drug Administration on Thursday proposed ending the use ... which is found in versions of drugs such as NyQuil, ...

The agency made the proposal after finding that the ingredient, known as oral phenylephrine, doesn’t relieve stuffy noses.

Despite needing FDA clearance to be on the shelves of your local pharmacy, some popular medicines probably don't work.

It was added to cold and flu remedies in the 1990s when another ingredient went behind the counter over illicit meth lab concerns.

Mucinex contains an active ingredient ... Guaifenesin is considered pregnancy category C by the U.S. Food and Drug Administration. That classification means means there's no data on human fetuses ...

If you have a bottle of Mucinex in your medicine cabinet, you may need to throw it away. Earlier this week, drugmaker RB recalled certain lots of over-the-counter Mucinex Fast-Max liquid products ...

“I took Mucinex 30 minutes before baby-dancing,” TikTok user Amanda MacGibbon shared in March. She said she also took the antioxidant supplement coenzyme Q10 and the anti-diabetic drug ...

Oxymetazoline HCl 0.05%; nasal spray; contains benzalkonium chloride, menthol, camphor, eucalyptol. <6yrs: not recommended. Shake well. ≥6yrs: 2–3 sprays in each nostril not more than every 10 ...

Dextromethorphan HBr 5mg, guaifenesin 100mg; per packet; orange creme flavor; contains (phenylalanine 2mg, magnesium 6mg, sodium 2mg) per packet. Empty entire contents of packet onto tongue and ...

The maker of Mucinex is working quickly after announcing ... Johnson & Johnson (NYSE: JNJ) subsidiary Janssen Biotech is planning to build a drug manufacturing facility in the city, which will ...