RegenESlim Appetite Control Capsules voluntarily recalled due to the presence of DMAA.

FDA warns consumers about caffeine powder. 

FDA advises consumers to stop using any supplement products labeled as OxyElite Pro or VERSA-1. Please see the following advisories: FDA -10/08/13, FDA - 10/11/13 and CDC - 10/08/13.

OPSS Hompage Button tall

Natural Medicines Homepage Button tall


New article on reporting side effects of supplements
Just published in The New England Journal of Medicine: A recent article brings up dietary supplement issues you need to be aware of and discusses how dietary supplement side effects could be monitored better. A PDF of the April 3rd article is available free online.

3rd International Congress on Soldiers’ Physical Performance
August 18-21, 2014
The ICSPP delivers innovative scientific programming on soldiers’ physical performance with experts from around the world.

DMAA list updated for April 2014

Fueling Performance Photo Campaign
Share photos of how you fuel your performance and be featured on our Facebook page!

Dietary supplement module
Earn continuing education credits (if eligible) for this two-hour online module.

Operation LiveWell

Performance Triad


HPRC's human performance optimization (HPO) website is for U.S. Warfighters, their families, and those in the field of HPO who support them. The goal is Total Force Fitness: Warfighters optimized to carry out their mission as safely and effectively as possible.

You are here: Home / Dietary Supplements / OPSS: Operation Supplement Safety / OPSS: Operation Supplement Safety / OPSS Frequently Asked Questions (FAQs) / Are there specific requirements for labeling of dietary supplement products?


Are there specific requirements for labeling of dietary supplement products?

OPSS Answer

FDA has very stringent and complex requirements for labeling (and marketing) of dietary supplement products. Most important is that FDA requires a “Supplements Facts” panel on all dietary supplement products. Although dietary supplements are generally classified as foods, they are required to have a “Supplements Facts” panel rather than the “Nutrition Facts” label required on conventional foods. FDA’s “How to Understand and Use the Nutrition Facts Label” web page has information that also applies to Supplement Facts panels. A dietary supplement product label should answer the following questions:

  • What is the name of the product?
  • How much product is in the package?
  • Who made/packed/distributed it?
  • What ingredients are in it?
  • What is the nutritional content?

The last two questions are answered by the Supplement Facts panel, which must identify ALL ingredients contained in the product and their amounts. However, some of the ingredients may be part of a mixture of ingredients, otherwise known as "proprietary blend", “blend” or “delivery system.” In this case only the total amount of the mixture of ingredients is required.

Updated 17 April 2014