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Dietary and Herbal Supplements. Federal law defines dietary supplements as products that: You take by mouth such as a tablet, capsule, powder, or liquid. Are made to supplement the diet. Have one or more dietary ingredients, including vitamins, minerals, herbs or other botanicals, amino acids, enzymes, tissues from organs or glands, or extracts of these.

Are labeled as being dietary supplements. Dietary supplements may interact with your medications or pose risks if you have certain medical problems or are going to have surgery. For example, some products marketed for weight loss, sexual enhancement, or bodybuilding have been found to contain prescription drugs not allowed in dietary supplements or other ingredients not listed on the label, and some of these ingredients may be unsafe.

Rules for manufacturing and distributing dietary supplements are less strict than those for prescription or over-the-counter drugs. Although the U. Food and Drug Administration FDA requires that companies submit safety data about any new ingredient not sold in the United States in a dietary supplement before , the FDA is not authorized to review dietary supplements for safety and effectiveness before they are marketed.

In , the FDA launched the Dietary Supplement Ingredient Directory , a webpage where the public can look up ingredients used in products marketed as dietary supplements and find what the FDA has said about that ingredient, as well as whether the agency has taken any action with regard to the ingredient.

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