The Food and Drug Administration is proposing a rule that cosmetic companies would have to take extra steps to ensure that ...
A Class I recall is used when "a violative product will cause serious adverse health consequences or death," according to the FDA.
If the proposed rule is finalized, cosmetic products would be considered adulterated under the Federal Food, Drug, and Cosmetic Act (FD&C Act) if a manufacturer fails to operate in compliance with ...
On Dec. 19, the FDA released the final rule on the use of “healthy” on food labels. Certain tea products now can display the ...
On Sept. 25, the U.S. Food and Drug Administration (FDA) hosted a public meeting to gather feedback on its proposed framework ...
WASHINGTON — Changes are coming to the cold and cough aisle of your local pharmacy: U.S. officials are moving to phase out ...
The United States Food and Drug Administration says the shortage of Eli Lilly’s Zepbound and Mounjaro drugs has been resolved ...
According to an FDA report, the proposed rule would mandate that manufacturers test each batch of talc-containing cosmetic products using advanced microscopy techniques, including polarized light ...
To qualify as healthy under the updated definition, food products must contain a certain amount of a food from at least one ...
Whole grains and fruits are in, and added sugar is out. That’s going to change what’s on a lot of cereal boxes and other things ...
The U.S. Food and Drug Administration has announced a final rule to update the definition of the nutrient content claim “healthy.” According to the ...
Manufacturers of baby powder and cosmetic products made with talc will have to test them for asbestos under a proposal announced by the U.S. Food and Drug Administration. The agency's proposal ...