Lead is toxic to people of any age or health status and higher exposure levels can lead to neurological changes ...

The alert follows a wave of warning letters the agency sent to Supergoop!, Vacation Inc. and three other popular brands, ...

The U.S. Food and Drug Administration has approved Tonix Pharmaceuticals' drug to manage pain related to a type of chronic condition called fibromyalgia, the company said on Friday. The approval paves ...

Under current regulations, oils, lotions, creams, gels, butters, pastes, ointments and sticks are the only forms of sunscreen ...

When U.S. regulators aren’t in the room while global standards are written, the future of patient safety, medical innovation, ...

Popular sunscreen products that come in mousse form, such as Supergoop!'s body mousse, may not protect wearers from the sun's ...

The U.S. Food and Drug Administration has approved Insmed's oral drug for a type of lung disease, the company said on Tuesday ...

More than 20 Republican attorneys general are demanding that the Trump administration reinstate safety protocols for the ...

The US Food and Drug Administration (FDA) is a prominent US federal governmental regulatory agency, headquartered in Silver Spring, Maryland. Its primary mission is to protect public health by ...

Dr Vinay Prasad will return to head the FDA’s Center for Biologics Evaluation and Research less than 2 weeks after being ousted.

The U.S. Food and Drug Administration (FDA) ban on GLP-1 compounding took effect on May 22, and the off-brand medications are no longer allowed to be made or sold in the United States.

While the FDA is working on removing the pots from shelves, it has been unable to initiate a mass recall, the agency warned.