The Food and Drug Administration approved on Friday a label change for Pfizer's birth control shot Depo-Provera that warns ...

Virginia Department of Agriculture and Consumer Services (VDACS) announced new regulations effective Jan. 1, 2026, requiring ...

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 FDA sent a letter to manufacturers of dietary supplements proposing a reduction in required warning labels.

FDA approves Depo-Provera label warning of meningioma brain tumor risk after 1983 studies; 1,000+ women sue Pfizer for ...

The FDA is removing a long-standing warning from hormone-based drugs used to treat menopause symptoms in women. FDA and HHS officials said the labels stemmed from a study published more than 20 years ...

FDA adds brain tumor warning to Depo-Provera label for Pfizer’s birth control injections after studies link the drug to meningioma risk.

The FDA is requiring manufacturers of opioid pain medications to update safety labels to better emphasize risks linked to their long-term use, the agency announced in a new Drug Safety Communication.

A label begins with highlights, a succinct, half-page summary of the information that health care practitioners most commonly refer to and view as most important (Figure 2). [4] This section provides ...