Dental Association Petitions FDA To Evaluate Tooth-Whitening Treatments
This article was originally published in The Rose Sheet
Executive Summary
The American Dental Association asks FDA to follow through on its promise to evaluate the safety of tooth-bleaching systems and classify the regulatory status of the products, which are rapidly increasing in number
You may also be interested in...
FDA Denies Petition To Classify Home Tooth Whiteners As Drugs
Data in a 2009 petition submitted by the American Dental Association is insufficient to warrant a drug designation for peroxide-containing tooth-whitening products as a group, according to the agency’s April 22 response. Further information on specific product formulations, mechanisms of action and safety profiles would be required for FDA to determine whether they meet the definition of a drug under federal law, the agency says.
P&G Defends Tooth-Whitening Cosmetic Classification In FDA Letter
Procter & Gamble urges FDA to deny a citizen petition by the American Dental Association to reclassify commercially available tooth whiteners as drugs, saying the petition is motivated by the financial interests of ADA members
P&G Defends Tooth-Whitening Cosmetic Classification In FDA Letter
Procter & Gamble urges FDA to deny a citizen petition by the American Dental Association to reclassify commercially available tooth whiteners as drugs, saying the petition is motivated by the financial interests of ADA members