![](https://webarchive.library.unt.edu/eot2008/20090119154448im_/http://www.fda.gov/graphics/dot_clear.gif) |
|
![](https://webarchive.library.unt.edu/eot2008/20090119154448im_/http://www.fda.gov/graphics/dot_clear.gif) |
March 11, 1999:
FDA publishes a regulation mandating that labels of all over-the-counter drugs contain information in a standardized, consumer-friendly format. These "Drug Facts" labels, similar in format to the Nutrition Facts label for foods, are designed to provide easy-to-find information to help patients use the product safely and effectively. |
|
|
|
The need for information about OTC medicines is growing: more than 700 medicine products available over-the-counter today use ingredients and dosages that were available only by prescription less than 30 years ago. There are more than 100,000 OTC |
|
products using about 1,000 active ingredients on the U.S market. The FDA offers a variety of resources to help consumers make good decisions about the OTC medicines they're using. |
|