To amend the Federal Food, Drug, and Cosmetic Act to establish rules regarding dietary supplements and for other purposes, Sec. Consequently, the DSHEA requires that when the label of a dietary supplement or other type of labeling includes such a statement, the statement must be accompanied by a disclaimer informing consumers that the FDA has not evaluated the claim. If you think you have suffered a harmful effect or illness (an adverse effect) from a dietary supplement, the first thing to do is to contact your healthcare provider or go to him immediately. DeFelice defined nutraceuticals as a wide variety of compounds that can be considered food or part of a food and that provide specific medical or health benefits, such as the prevention and treatment of diseases or the improvement of physiological performance (Brower, 1998; Kalra, 200).
While the general objective of GMPs for foods and dietary supplements is the same, namely, to regulate the manufacture of such products in a way that helps ensure the safety of the food supply, the regulations applicable to each specific category of food differ substantially. As building blocks of cartilage, glycosaminoglycans are naturally produced by the human body, but they can also be supplemented by diet. The law gives the FDA adequate regulatory authority and extensive enforcement tools to protect consumers while allowing them the desired access to a wide variety of affordable, high-quality, safe and beneficial dietary supplements. However, by law, the FDA does not approve dietary supplements or their labeling, although certain types of claims that are sometimes used in the labeling of dietary supplements require pre-market review and authorization (e.g., despite the regulatory status of dietary supplements for animal use, there are many products on the market that contain unapproved feed ingredients).
The Dietary Supplements Health and Education Act (DSHEA) amended the Federal Food, Drug, and Cosmetic Act (FD&C Act) to create a new regulatory framework for dietary supplements. Consumers can contact the manufacturer of the dietary supplements or a commercial laboratory to analyze the content of a product. In the preamble to the final regulation on good manufacturing practices for dietary supplements, the FDA expressly indicated that article 111 of the Food Regulatory Code (21 CFR, part 111) does not apply to companies that manufacture and supply only dietary ingredients. To be a dietary supplement, a product must also be labeled as a dietary supplement; that is, the product label must include the term dietary supplement or equivalent (e.g., you can find more information on reporting adverse events associated with the use of dietary supplements in How to Report a Problem with Dietary Supplements).
The CVM and state feed control officials also regulate the distribution of nutritional supplements for animals. CS and G, alone or in combination, are the oral supplements most commonly taken to improve joint health in people with arthritis.