Dietary supplements are regulated by the FDA as foods, not as medicines. However, many dietary supplements contain ingredients that have strong biological effects that may conflict with a drug you are taking or with a medical condition you may have. The FDA is not authorized to review dietary supplement products for safety and effectiveness before they are marketed. The law defines dietary supplements in part as products that are taken orally and contain a dietary ingredient.
Dietary ingredients include vitamins, minerals, amino acids, and herbs or botanicals, as well as other substances that can be used to supplement the diet. The FDA receives many consumer inquiries about the validity of dietary supplement claims, including product labels, advertisements, media, and print materials. Dietary supplements come in many forms, including tablets, capsules, powders, energy bars, and liquids. Prior to 1994, dietary supplements were subject to the same regulatory requirements as FDA foods.
And some of them have had dramatic effects on supplement sales and supplement use, Dr. For a general complaint or concern about food products, including dietary supplements, you can contact the consumer complaint coordinator at the local FDA district office closest to you. Before taking a dietary supplement, make sure that the supplement is safe for you and appropriate for its intended purpose. Because dietary supplements fall under the umbrella of food, the FDA's Center for Food Safety and Applied Nutrition (CFSAN) is responsible for the agency's oversight of these products.
Current FDA regulations only require “reasonable assurances that dietary supplements do not pose “a significant or unreasonable risk of illness or injury when the product is used as directed, or with regular use if the label does not include instructions. That's why I “strongly advise people to talk to their doctors about supplements, because “using inappropriate supplements can lead to several problems, Dr. First, because dietary supplements are usually prescribed on their own or are available over the counter, medical professionals don't constantly monitor for negative side effects. In October 1994, President Clinton enacted the Dietary Supplements Health and Education Act (DSHEA).
For example, some interested parties have suggested amending the statute to establish avenues for the exclusivity of dietary supplements and add a product listing requirement. The FDA regulates dietary supplements under a different set of regulations than those covered by conventional foods and pharmaceuticals. Anyone can report a serious adverse event or illness that is considered to be related to a dietary supplement directly to the FDA by accessing the SRP listed above.
