Dietary Supplement Database Fda

Fda is unable to test and identify all products marketed as dietary supplements on the market that have potentially harmful hidden ingredients.

Dietary supplement database fda. Food and drug. The manufacturer or distributor is responsible for this label information and the office of dietary supplements ods does not check or verify that it conforms to u s. A dietary supplement is a product taken by mouth that contains a dietary ingredient intended to supplement the diet the fda adds that the dietary ingredients inside supplements can include vitamins minerals herbs or other botanicals amino acids and substances such as enzymes organ tissues glandulars and.

To contact the office of dietary supplement programs email. The cfsan adverse event reporting system caers is a database that contains information on adverse event and product complaint reports submitted to fda for foods dietary supplements and cosmetics. Even if a product is not included in this list consumers should exercise caution before using certain products.

The dietary supplement ingredient database dsid provides estimated levels of ingredients in dietary supplement products sold in the united states. Food and drug administration fda announced regulations that require amendments to the existing supplement facts label which uses units and conversions based on the 1968 recommended daily allowances rda. To contact the office of dietary supplement programs email.

Office of dietary supplement programs hfs 810 food and drug administration 5001 campus dr college park md 20740. These statistically predicted estimates may differ from labeled amounts and are based on chemical analysis of nationally representative products. The new regulations will be mandatory in 2019 2020.

The dietary supplement label database dsld is intended to capture all information from the labels of products sold as dietary supplements in the united states. 1 888 safefood 1 888 723 3366 content current as of. Odsp fda hhs gov to reach fda s food and cosmetics information center call.

The database can be used to evaluate fda s warning letter allegations of good manufacturing practices gmps violations products making impermissible claims and products.