The FDA is weighing a change that could make warning labels on dietary supplements appear less often on packaging.

WASHINGTON D.C. —The U.S. Food and Drug Administration is mandating safety changes to opioid pain medication labels, a move officials say will better warn patients and prescribers about the risks of ...

The FDA is considering a rule change that would cut back on how often dietary supplement warnings must appear on packaging, a move experts say could make them easier to miss.

The U.S. Food and Drug Administration is reviewing whether to change the warning label on hormone replacement therapy drugs used to treat menopause symptoms, a move many experts say is long overdue.

The US Food and Drug Administration (FDA) has instructed all GLP-1 drug-makers to update their warning labels to include the risk of serious kidney injury that can result from dehydration. This comes ...

(Washington-AP) Jan. 19, 2006 - Two prescription creams for eczema will soon carry cancer warnings. The Food and Drug Administration is ordering the makers of the ointments Elidel and Protopic to add ...

Supplements are not reviewed by the U.S. Food and Drug Administration before they are sold The FDA may allow warning labels to appear just once per package rather than after every health claim Some ...

The U.S. Food and Drug Administration (FDA) is weighing a change that could make warning labels on dietary supplements appear less often on packaging. Unlike prescription drugs, dietary supplements ...

Under a possible rule change outlined in a letter sent to supplement makers, the FDA would still require that warning on the package, but only once, rather than next to every health claim. HealthDay ...