Dietary Supplement Regulation †
DSHEA (1994) is important legislation, passed by the US Congress, to amend the Federal Food, Drug, and Cosmetic Act (1938); further defining supplement industry standards, regulation, and safe manufacture. In 2000, further rulings, for supplements by the Food and Drug Administration (FDA) regulate them solely as food and not drugs for medical use.
Dietary Supplements are Food Added to a Complete Diet †
Types of Supplements
Dietary supplements are any combination of the following:
- Amino Acids
Concentrates, Metabolites, or Extracts from foods.
Supplements are Regulated to Promote Educational Health Claims
Supplement regulation promotes and sells supplements by educating the buyer in how they support health and well-being in non-medical ways. Currently accepted non-disease and non-health-condition claims for dietary supplements include:
Research Dietary Supplements with Health Education †
- General Health and Wellness
- Nutrient Content
General health and wellness: A supplement with general health and wellness benefits, shown by historical use (e.g. tradition and herbalism) and/or with reliable scientific evidence (e.g. biochemistry, nutrient science, and herbal medicine). Examples: Ginger concentrate has traditionally been used medicinally for digestion; Skullcap has been used in herbalism as a calming medicinal remedy.
Nutrient content: Show specific nutrients are present within a supplement (e.g. vitamins, minerals, & amino acids). Books and scientific literature provide reliable and valid evidence for nutrient content claims in supplements. Examples: Goji berry extracts contain beta-carotene which is good for the eyes; Amla berry contains vitamin c which is good for the immune system.
Structure/Function: Scientific literature shows how any nutrient or constituent of a supplement works within the metabolic processes of a structure and/or function of the body. In other words, a supplement has structure/function benefits when it is concentrated and/or metabolized within a system, organ, gland, fluid, or tissue. Examples: Calcium promotes bone health; Omega-3 fatty acids maintain heart health; Salt supports stomach acid for digestion.
Importantly, medical studies may be used because they use the scientific method, including animal or human studies, observational studies and/or clinical trials. Find information about the structure/function benefits of supplements when using a medical study, instead of using it to confirm a drug-like mechanism of intervention; thereby excluding the irrelevant disease or unrelated health-condition conclusions.
Manufactures Use Health Education in Supplement Promotion
The DSHEA (1994) prevents individual manufactures from making exclusive claims about the effectiveness of their own branded supplements. Instead manufactures make general claims (i.e., traditional uses, health education, & scientific methods) of the health benefits of the types of supplements that they manufacture.
The Food and Drug Administration (FDA) Regulation Limitations for Disease Related Health Claims
Note that final rulings in 2000 from the FDA have greatly limited the scope of the US Congress' passage of DSHEA (1994) and vastly reduced the FDA's own ability to approve and promote foods and supplements with intended medical use in the treatment, prevention, and management of diseases and health-conditions; by disallowing all unapproved disease and health-condition claims for foods and supplements. Approved disease and health-condition claims are sometimes confusingly known as health claims within agency documentation.
Non-Deceptive Supplement Promotion
The DSHEA (1994) requires any published health supporting claims with dietary supplements be presented as truthful, and not misleading, according to accepted non-medical understanding, including traditional uses, health education, and scientific methods of research.
Under FDA agency ruling in January (2000), regulation was established that all claims for dietary supplements cannot suggest disease and health-conditions related prevention, treatment, and management effects, unless they are agency approved as a qualified health claim.
Be Aware of Dietary Supplement Disinformation †
The Federal Trade Commission (FTC) works with the FDA to offer guidance in avoidance of deceptive advertising for supplements.
DSHEA (1994) for Safe Manufacture of Supplements
The DSHEA (1994) authorizes US government and the FDA agency regulatory oversight to set the requirements for safe supplement manufacture, which is known as Current Good Manufacturing Practice (CGMP); based on food processing and procedures, including sanitation, packaging, and labeling.
The DSHEA (1994) for a Thriving Supplement Industry
Ultimately, the DSHEA (1994) is regulation passed by the US Congress to encourage the supplement industry to promote health education with the sale of dietary supplements without medical quackery and without interference or corruption from the pharmaceutical industry.
Combined, the DSHEA (1994) legislation and FDA rulings regulate the FDA by prohibiting the FDA from approving foods and supplements as drugs, while also prohibiting anyone from promoting, selling, and using foods and supplements wrongly as drugs and medical treatments for the prevention, management, and cure of diseases and health-conditions.