• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

About FDA

  • Print
  • Share
  • E-mail

FDA Basics Webinar on Reporting Adverse Events Related to Cosmetics

 

From morning until night—styling our hair for work to showering before bed—Americans depend upon personal care products. Most are safe, but some may cause problems, and that’s when FDA gets involved. FDA collects information about consumers’ adverse events for products it regulates. These reports are important to our understanding of the effects of cosmetics on public health.
 

FDA hosted a webinar, “Cosmetic Adverse Event Reporting," Wednesday, January 18th at 2:00 p.m. ET. Interdisciplinary Scientist Wendy Good and Policy Fellow Jon Hicks, of FDA's Office of Cosmetics and Colors, provided information on how FDA regulates cosmetics and monitors their safety, ways to reduce risks to consumers, how to report a bad reaction to a cosmetic, and how this information helps FDA in its public health mission. They also talked about steps consumers can take to minimize the chances of having a bad reaction to a cosmetic. 
 
An archived version of this presentation will be available shortly
 
You can download slides of the presentation here: Cosmetic Adverse Event Reporting (PDF 938 KB)

 

Additional Resources:

Consumer Update: Bad Reaction to Cosmetics? Tell FDA

 

 

Basics Question toggle Show all related FDA Basics Questions

-

How helpful was this information?

                               

Not HelpfulArrow pointing to the rightVery Helpful


Please limit your feedback to 1000 characters.

Please limit your feedback to 1000 characters.

If you would like to ask a specific question, please visit our "Contact Us" page for more information about how to contact FDA.

Please note that any information you submit may become public or subject to release under the Freedom of Information Act (FOIA). For more information, read about our privacy policies and the FOIA.

-