What are the FDA’s standards for safety and effectiveness of dietary supplements?

The FDA, or the U.S. Food and Drug Administration, has established rigorous standards to ensure the safety and effectiveness of dietary supplements. These standards are in place to protect consumers and promote overall well-being.

Safety Standards

Before a dietary supplement can be marketed in the United States, the FDA requires manufacturers to provide evidence that the product is safe for consumption. Manufacturers must conduct thorough safety assessments and provide data to support the safety of the ingredients used in the supplements.

Effectiveness Standards

In addition to safety standards, the FDA also requires evidence of effectiveness for dietary supplements. Manufacturers must provide data to demonstrate that the product delivers the benefits claimed on the label.

Regulations and Criteria

The FDA regulates dietary supplements under the Dietary Supplement Health and Education Act of 1994. This act sets forth regulations regarding ingredients, labeling, and manufacturing practices for dietary supplements. Manufacturers are required to adhere to good manufacturing practices (GMP) to ensure quality control and consistency in their products.

In conclusion, the FDA's standards for safety and effectiveness of dietary supplements are designed to safeguard consumers and promote their well-being by ensuring that supplements are safe, effective, and of high quality.