The Food and Drug Administration (FDA) announced Wednesday it will ban Red No. 3, a common artificial food dye linked ...

A Class I recall is used when "a violative product will cause serious adverse health consequences or death," according to the FDA.

Indonesia entry into BRICS marks a strategic milestone for its domestic economy and global trade landscape, said Alexander Michael Tjahjadi, an ...

The FDA banned the use of Red Dye No. 3 based on a petition asking that the agency follow a specific guideline.

president of the Center for Science in the Public Interest and a former FDA official, said in a statement. “But the truth is Congress made plain decades ago that this was exactly the type of ...

The U.S. Food and Drug Administration has approved AstraZeneca and partner Daiichi Sankyo's precision drug to treat a type of ...

The FDA proposes front-of-package nutrition labels to help consumers quickly identify levels of saturated fat, sodium, and added sugars in packaged foods.

To help combat the nation’s chronic disease crisis, the FDA has announced a proposal for a rule that would require front-of-package labeling for nutritional information. If finalized ...

The FDA’s influential director of the Center for Drug Evaluation and Research, Patrizia Cavazzoni, M.D., will soon retire from the agency. The seven-year FDA veteran communicated the decision in ...

"The FDA cannot authorize a food additive or color additive if it has been found to cause cancer in human or animals," Jim Jones, the FDA's deputy director for human foods, said in a statement.

Opens in a new tab or window Share on LinkedIn. Opens in a new tab or window In its final days, the Biden administration's FDA is expected to propose a limit on the amount of nicotine in cigarettes.

Officials cited a statute known as the Delaney Clause, which requires FDA to ban any additive found to cause cancer in people or animals. The dye is known as erythrosine, FD&C Red No. 3 or Red 3.