An off-brand version of Dayquil and Nyquil has been recalled due to substandard quality. Last week, the U.S. Food and Drug Administration (FDA) recalled 8,640 boxes of Kirkland Signature Severe Cold & ...

A U.S. Food and Drug Administration panel has concluded that a common decongestant does not effectively relieve cold and allergy symptoms, setting up a possible recall of many popular medicines.

The Food and Drug Administration (FDA) is proposing to remove from the market a common ingredient found in most oral over-the-counter cold medicines because it doesn’t work. The move brings FDA one ...

The agency now must decide whether products containing the ingredient, like some Sudafed and NyQuil products, should no longer be sold or perhaps give companies lead time to substitute other ...

Cold and flu medicine sits on a store shelf Tuesday in Florida. A Food and Drug Administration advisory panel announced an ingredient in many over-the-counter cold and allergy medications called ...

SALT LAKE CITY (KUTV) — Three Utah residents have sued major cold medicine manufacturers over products containing phenylephrine, an ingredient that has been deemed ineffective as a nasal decongestant ...

CINCINNATI (WKRC) - The Food and Drug Administration (FDA) is considering removing oral phenylephrine, a common ingredient in many over-the-counter cold and flu medications, after determining it is ...