Earlier this month, the U.S. Food and Drug Administration proposed food companies use new, front-of-package labels highlighting the levels of fat, salt and added sugar in their products.
PROVIDENCE — Katelyn Holt has been a nurse for over a decade. Throughout her career, she has noticed that the catheters her ...
Wetherill to lead the Division of Chemistry, which would become the Bureau of Chemistry in 1901 and the Food and Drug Administration in 1906. 1906 – Pure Food and Drug Act and Federal Meal Inspection ...
Moreover, it's not always easy to get information on the safety ... as well as the relevant part of the U.S. Food and Drug Administration's Food Code. (Iowa refers to the 2017 edition of Food ...
The Food and Drug Administration (FDA ... Finally, we expect that digital health and data privacy will continue to draw intense scrutiny from health regulators in the foreseeable future.
The Food and Drug Administration (FDA or we) is amending the color additive regulations to provide for the safe use of myoglobin as a color additive in ground meat and ground poultry analogue products ...
VHG Labs DBA LGC Standards has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Companies say they are working to update their products to comply with the Food and Drug Administration's decision Wednesday to ban the artificial food dye Red 3, after the agency said it was ...
Manufacturers will no longer be allowed to use the dye, called red No 3 or red dye 3, after studies linked it to cancer in male laboratory rats, the US Food and Drug Administration (FDA ...
On Wednesday, the Food and Drug Administration (FDA) proscribed the dye based on a 2022 petition by consumer advocacy groups against its use, which had already been banned in cosmetics 35 years ago.
An increase in sulfite allergies led the U.S. Food and Drug Administration (FDA) to ban their use in fresh vegetables and fruits back in 1986. Today, food manufacturers must declare on product labels ...
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