FDA published two final guidance documents related to food allergens: Questions and Answers Regarding Food Allergens, ...
On January 7, 2025, the US Food and Drug Administration (FDA) issued two parallel guidance documents for the Section 503A and Section 503B bulk ...
The revised prescription drug labeling developed by the Food and Drug Administration (FDA) is described. Summary: A new FDA final rule, "Requirements on Content and Format of Labeling for Human ...
The FDA has escalated a chocolate recall to its highest risk level, citing life-threatening dangers for those with allergies.
The Food and Drug Administration uses import alerts to enforce U.S. food safety regulations for food from foreign countries. The agency updates and ...
Medical experts and death row inmates file legal briefs challenging legality of Arizona's execution drugs ahead of March ...
A voluntary recall was initiated by The W.S. Badger Company due to missing labels on a sunscreen product distributed nationwide.
The FDA issued a warning letter to ProRx, a compounding facility in Exton, Penn., after an inspection raised serious concerns regarding the safety and compliance of its drug products. The facility, ...
Pro-choice advocates say the science is settled on the abortion pill mifepristone, but critics argue that better safeguards ...
Most states allow some sale of cannabis, but testing for pesticides and mold in the weed supply varies from one state to ...
There’s nothing fishy about this skincare secret — unless you count the ingredients. The pursuit of plastic-free perfection ...
USE ONAPGO is a prescription medicine used to treat motor fluctuations (OFF episodes) in adults with advanced Parkinson’s disease (PD). It is not known if ONAPGO is safe and effective in children.