CFSAN Constituent Update - Using Adverse Event Reports to Monitor Cosmetic Safety

[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]

 



Title: CFSAN Constituent Update - Using Adverse Event Reports to Monitor Cosmetic Safety

FDA Logo

Center for Food Safety and Applied Nutrition

Constituent Update


Using Adverse Event Reports to Monitor Cosmetic Safety

December 8, 2016

It’s not an exaggeration to say that everyone uses cosmetics, be it shampoo, mouthwash, a moisturizer or deodorant. The FDA monitors cosmetics on the market to ensure that they are safe for consumers.

One way in which FDA finds out about a safety issue is when an adverse event report (AER) is filed by a consumer, manufacturer, or health care professional. An adverse event could be any problem experienced when using a cosmetic product. On Tuesday, Dec. 6, 2016, FDA announced that it is making public certain data that the agency’s Center for Food Safety and Applied Nutrition (CFSAN) receives about adverse events associated with the use of its regulated products, which include cosmetics.

Linda Katz, M.D., MPH, director of FDA’s Office of Cosmetics and Colors, talks about some of the safety issues involving cosmetics, how FDA is responding to them, and how consumers interested in safety data about cosmetics can best use information in the CAERS database.

For More Information:


This email was sent to list-fda@xxxxxxxxxxx using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332) Powered by GovDelivery

[Index of Archives]     [CDC News]     [NIH News]     [USDA News]     [Steve's Art]     [Camping in Yosemite]     [PhotoForum]     [SB Lupus]     [STB]

  Powered by Linux