Dietary supplements contain ingredients like vitamins, minerals, herbs and other botanicals. They come in various forms such as tablets, capsules, and powders. A dietary supplement is defined as a product intended to supplement the diet that contains one or more dietary ingredients. Supplements can provide benefits like obtaining vital substances, reducing disease risk, and not replacing complete meals. However, risks include supplements interacting harmfully with other supplements, medications, or being overused. Supplement labels must include information like product name, quantity, and manufacturer but are not required to be approved by the FDA for safety and effectiveness.
2. WHAT ARE DIETARY SUPPLEMENTS
Contain ingredients such as
Vitamins, Minerals
Herbals, Botanicals
Amino acids
Enzymes
Come in the following forms
Tablets
Capsules
Softgels
Gelcaps
Powders and liquids
Definition of a Dietary Supplement was defined by
Congress due to the Dietary Supplement Health
and Education Act; which became law in 1994
3. BENEFITS & RISKS OF SUPPLEMENTS
Benefits
Get enough vital substances for the body to function
Helps reduce the risk of disease
Not to replace complete meals
Risks
Supplements can be harmful to the body or even life threatening when
Combined with other supplements
Using supplements with medications
Substituting supplements for prescription medications
Taking too many supplements of one kin
4. DIETARY SUPPLEMENT CLAIMS
Can contain one of three claims
Health claim: a statement that describes a relationship between food, food component, or dietary supplement
ingredient and the reduction in risk of developing a disease or health-related condition
Nutrient content claim: a statement label that describes the amount of a nutrient or dietary substance in a product
Structure/function claim: a statement label that describes how a product may affect the organs or systems of the
body; a specific disease cannot be mentioned
Dietary supplements cannot claim they treat, diagnose, prevent or cure disease
5. LABELING & REGULATION
Labeling
FDA requires the following on a label
Name of product
Net quantity of contents
Name and place of business, manufacturer, packer
or distributor
Directions for use
Serving size
Proprietary blend
Other ingredients
Label must contain a cautionary statement
Label does not determine the quality of the
product
Regulation
FDA regulates dietary supplements as well as
the labels and claims
There are no provisions in law for the FDA to
approve the safety and effectiveness of dietary
supplements
Are not required to be standardized in the
United States
Standardization is a process done by the
manufacturers and provides a measure of
quality control
6. REFERENCES
National Institutes of Health, Office of Dietary Supplements, US Department of Health and Human
Services, (2017). Retrieved online at
https://ods.od.nih.gov/Health_Information/ODS_Frequently_Asked_Questions.aspx
US Food and Drug Administration. Food. Dietary Supplements. US Department of Health and Human
Services, (2017). Retrieved online at https://www.fda.gov/Food/DietarySupplements/ucm2006892.htm