Warning Letters Related to Cosmetics
FDA issues Warning Letters to let companies know that they have violated the laws we enforce and to tell them what corrective action they need to take.
Matters described in FDA Warning Letters may have been subject to subsequent interaction between FDA and the recipient of the letter that may have changed the regulatory status of the issues discussed in the letter. If you would like to obtain available additional information on the current status of an issue in a particular Warning Letter on this website, please contact FDA or the recipient of the letter directly. Inquiries to FDA should be sent to: Food and Drug Administration Division of Freedom of Information (HFI-35), 5600 Fishers Lane, Rockville, MD 20857. Instructions for submitting an FOI request are available online.
- Warning Letters Address Drug Claims Made for Products Marketed as Cosmetics Updated October 31, 2012
- Warning Letters Cite Cosmetics as Adulterated Due to Microbial Contamination Updated August 21, 2012
- Warning Letters Highlight Differences Between Cosmetics and Medical Devices Updated April 28, 2011
- Warning Letter Cites Brazilian Blowout for Safety and Labeling Violations August 22, 2011
- Warning Letter to Procter and Gamble (Olay LLC) Cites Inadequate Manufacturing Conditions April 24, 2009
- Warning Letter to Black Henna Ink, Inc. Cites Illegal Use of Color Additive August 14, 2006
- Warning Letter to Parnell Pharmaceuticals, Inc. Cites Oral Moisturizer as Adulterated and Misbranded Medical Device July 10, 2006
- Warning Letters Cite Cosmetics as Adulterated Due to Violative Use of Canthaxanthin April 5, 2005
- Recalls and Alerts
- Is It a Cosmetic, a Drug, or Both? (Or Is It Soap?)
- FDA Authority Over Cosmetics
- Key Legal Concepts: Interstate Commerce, Adulterated, and Misbranded