Dietary supplements are a topic of great public interest. Whether you are in a store, using the Internet, or talking to people you know, you may hear about supplements and claims of benefits for health. How do you find out whether "what's in the bottle" is safe to take, and whether science has proven that the product does what it claims? This fact sheet provides some answers.
1. What are dietary supplements?
About Dietary SupplementsA dietary supplementA product that contains vitamins, minerals, herbs or other botanicals, amino acids, enzymes, and/or other ingredients intended to supplement the diet. The U.S. Food and Drug Administration has special labeling requirements for dietary supplements and treats them as foods, not drugs. must meet all of the following conditions:
Dietary supplements are sold in grocery, health food, drug, and discount stores, as well as through mail-order catalogs, TV programs, the Internet, and direct sales.
People take supplements for many reasons. A scientific study on this topic was published in 2002.3 In it, over 2,500 Americans reported on supplements they used (given the categories of vitamins/minerals and herbal products/natural supplements) and for what reasons. Their responses are summarized in the table below.
|Supplements: Why Taken?|
|Health/good for you||35||Health/good for you||16|
|Vitamin/mineral supplement||8||Memory improvement||6|
|Physician recommended||6||Immune booster||5|
|Don't know/no reason specified||3||Supplement diet||4|
|Immune booster||2||Sleep aid||3|
|Recommended by friend/family/media||2||Prostate||3|
|Energy||2||Don't know/no reason specified||2|
|All others||22||All others||45|
3. Is using supplements considered conventional medicineMedicine as practiced by holders of M.D. (medical doctor) or D.O. (doctor of osteopathy) degrees and by their allied health professionals such as physical therapists, psychologists, and registered nurses. or complementary and alternative medicine (CAM)A group of diverse medical and health care systems, practices, and products that are not presently considered to be part of conventional medicine. Complementary medicine is used together with conventional medicine, and alternative medicine is used in place of conventional medicine.?
Some uses of dietary supplements have become part of conventional medicine (see box below). For example, scientists have found that the vitamin folic acid prevents certain birth defects, and a regimen of vitamins and zinc can slow the progression of the eye disease age-related macular degeneration.
On the other hand, some supplements are considered to be CAM--either the supplement itself or one or more of its uses. An example of a CAM supplement would be an herbal formula that claims to relieve arthritis pain, but has not been proven to do so through scientific studies. An example of a CAM use of a supplement would be taking 1,000 milligrams of vitamin C per day to prevent or treat a cold, as the use of large amounts of vitamin C for these purposes has not been proven.
There are several ways to get information on supplements that is based on the results of rigorous scientific testing, rather than on testimonials and other unscientific information.
- Ask your health care provider. Even if your provider
does not happen to know about a particular supplement,
he can access the latest medical guidance about
its uses and risks.
- Dietitians and pharmacists also have helpful information.
- You can find out if there are any scientific research findings on the CAM supplement in which you are interested. NCCAM and other Federal agencies have free publications, clearinghouses, and databases with this information.
Here are some points to keep in mind:
- Tell your health care providers about any complementary
and alternative practices you use. Give them a full
picture of what you do to manage your health. This
will help ensure coordinated and safe care. It is
especially important to talk to your provider
- Are thinking about replacing your regular
medical care with one or more supplements.
- Are taking any medications (whether prescription
or over-the-counter). Some supplements have
been found to interact with medications (see
- Have a chronic medical condition.
- Are planning to have surgery. Certain supplements
may increase the risk of bleeding or affect
anesthetics and painkillers.
- Are pregnant or nursing a baby.
- Are considering giving a child a dietary supplement.
Supplements can act like drugs, and many have
not been tested in pregnant women, nursing mothers,
- Are thinking about replacing your regular medical care with one or more supplements.
- Do not take a higher dose of a supplement than
what is listed on the label, unless your health
care provider advises you to do so.
- If you experience any side effects that concern
you, stop taking the supplement, and contact your
provider. You can also report your experience to
the U.S. Food and Drug Administration's (FDA) MedWatch
program, which tracks consumer safety reports on
- If you are considering or using herbal supplements
--type of dietary supplement that contains herbs,
either alone or in mixtures., there are some
special safety issues to consider.
- For current information from the Federal Government
on the safety of particular supplements, check the
"Alerts and Advisories" section of the
NCCAM Web site or the FDA Web site.
Supplements and Drugs Can Interact
There are many supplements, as well as many prescription drugs, that come from natural sources and are both useful and safe. However, "natural" does not always mean "safe" or "without harmful effects." For example, consider mushrooms that grow in the wild--some are safe to eat, while others are poisonous.
The FDA issues warnings about supplements that pose risks to consumers, including those used for CAM therapies. A sample list is in the box below6,7. The FDA found these products of concern because they:
- Could damage health--in some cases severely.
- Were contaminated--with other unlabeled herbs,
pesticides, heavy metals, or prescription drugs.
- Interacted dangerously with prescription drugs.
Examples of Supplements
Yes, the Federal Government regulates supplements through the FDA. Currently, the FDA regulates supplements as foods rather than drugs. In general, the laws about putting foods (including supplements) on the market and keeping them on the market are less strict than the laws for drugs. Specifically:
- Research studies in people to prove a supplement's
safety are not required before the supplement
is marketed, unlike for drugs.
- The manufacturer does not have to prove that the
supplement is effective, unlike for drugs.
The manufacturer can say that the product
addresses a nutrient deficiency, supports health,
or reduces the risk of developing a health problem,
if that is true. If the manufacturer does make a
claim, it must be followed by the statement "This
statement has not been evaluated by the Food and
Drug Administration. This product is not intended
to diagnose, treat, cure, or prevent any disease."
- The manufacturer does not have to prove supplement
- The FDA does not analyze the content of dietary
- At this time, supplement manufacturers must
meet the requirements of the FDA's Good Manufacturing
Practices (GMPs) for foods. GMPs describe conditions
under which products must be prepared, packed,
and stored. Food GMPs do not always cover all
issues of supplement quality. Some manufacturers
voluntarily follow the FDA's GMPs for drugs,
which are stricter.
- Some manufacturers use the term "standardized"
to describe efforts to make their products consistent.
However, U.S. law does not define standardization.
Therefore, the use of this term (or similar
terms such as "verified" or "certified") does
not guarantee product quality or consistency.
- The FDA does not analyze the content of dietary supplements.
- If the FDA finds a supplement to be unsafe once
it is on the market, only then can it take action
against the manufacturer and/or distributor, such
as by issuing a warning or requiring the product
to be removed from the marketplace.
In March 2003, the FDA published proposed guidelines for supplements that would require manufacturers to avoid contaminating their products with other herbs, pesticides, heavy metals, or prescription drugs. The guidelines would also require supplement labels to be accurate.
The Federal Government also regulates supplement advertising, through the Federal Trade Commission. It requires that all information about supplements be truthful and not mislead consumers.
What's in the Bottle Does Not Always Match What's on the Label
A supplement might:
Yes, NCCAM is funding most of the nation's current research aimed at increasing scientific knowledge about supplements--including whether they work; if so, how they work; and how purer and more standardized products could be developed. Among the substances that researchers are studying are:
- Yeast-fermented rice, to see if it can lower cholesterol
levels in the blood
- Ginger and turmeric, to see if they can reduce
inflammation associated with arthritis and asthma
- Chromium, to better understand its biological
effects and impact upon insulin in the body, possibly
offering new pathways to treating type 2 diabetes
- Green tea, to find out if it can prevent heart
Recent NCCAM-sponsored or cosponsored clinical trials include:
- Glucosamine hydrochloride and chondroitin
--substance found in the cartilage around joints.
Chondroitin in dietary supplements is made in the
laboratory or from the cartilage of sharks and cattle.
sulfate, to find out if they relieve knee pain from
- Black cohosh, to see if it reduces hot flashes
and other symptoms of menopause
- Echinacea, to see if it shortens the length or
lessens the severity of colds in children
- Garlic, to find out if it can lower moderately
high cholesterol levels
- Ginkgo biloba, to determine whether it
prevents or delays decline in cognitive (thinking)
function in people aged 85 or older
- Ginger, to confirm whether it eases nausea and
vomiting after cancer chemotherapy
1. Dietary Supplement Health and Education Act of 1994. Food and Drug Administration Web site. Accessed at fda.gov/opacom/laws/dshea.html on April 14, 2003.
2. Dietary supplements: overview. U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition Web site. Accessed at cfsan.fda.gov/~dms/supplmnt.html on August 20, 2003.
3. Kaufman DW, Kelly JP, Rosenberg L, et al. Recent patterns of medication use in the ambulatory adult population of the United States: the Slone survey. Journal of the American Medical Association. 2002;287(3):337-344.
4. Federal Trade Commission. Promotions for kids' dietary supplements leave sour taste. Federal Trade Commission Web site. Accessed at ftc.gov/opa/2004/06/kidsupp.htm on May 2, 2003.
6. MedWatch: the FDA safety information and adverse event reporting program. U.S. Food and Drug Administration Web site. Accessed at fda.gov/medwatch on August 20, 2003.
7. Dietary supplements: warnings and safety information. U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition Web site. Accessed at cfsan.fda.gov/~dms/ds-warn.html on April 14, 2003.
For More Information
The NCCAM Clearinghouse provides information on CAM
and NCCAM, including publications and searches of
Federal databases of scientific and medical literature.
The Clearinghouse does not provide medical advice,
treatment recommendations, or referrals to practitioners.
Toll-free in the U.S.: 1-888-644-6226
TTY (for deaf and hard-of-hearing callers): 1-866-464-3615
Web site: nccam.nih.gov
U.S. Food and Drug Administration (FDA)
The FDA oversees the safety of many products, such
as foods (including dietary supplements), medicines,
medical devices, and cosmetics.
Web site: fda.gov
Toll-free in the U.S.: 1-888-463-6332
Center for Food Safety and Applied Nutrition (CFSAN)
CFSAN oversees the safety and labeling of supplements,
foods, and cosmetics. Publications include "Tips
for the Savvy Supplement User: Making Informed Decisions
and Evaluating Information."
Web site: cfsan.fda.gov
Toll-free in the U.S.: 1-888-723-3366
MedWatch, the FDA's safety information and adverse
event reporting program, allows consumers and health
care providers to file reports on serious problems
suspected with dietary supplements.
Web site: fda.gov/medwatch/report/consumer/consumer.htm
Toll-free in the U.S.: 1-888-463-6332
Federal Trade Commission (FTC)
The FTC is the Federal agency charged with protecting
the public against unfair and deceptive business practices.
A key area of its work is the regulation of advertising
(except for prescription drugs and medical devices).
Web site: ftc.gov
Toll-free in the U.S.: 1-877-382-4357
Office of Dietary Supplements (ODS), NIH
ODS seeks to strengthen knowledge and understanding
of dietary supplements by evaluating scientific information,
supporting research, sharing research results, and
educating the public. Its resources include publications
and the International Bibliographic Information on
Dietary Supplements (IBIDS) database.
Web site: ods.od.nih.gov
A service of the National Library of Medicine (NLM),
PubMed contains publication information and (in most
cases) brief summaries of articles from scientific
and medical journals. CAM on PubMed, developed jointly
by NCCAM and NLM, is a subset of the PubMed system
and focuses on the topic of CAM.
Web site: ncbi.nlm.nih.gov/entrez
CAM on PubMed: nccam.nih.gov/camonpubmed/
The Cochrane Database of Systematic Reviews
The Cochrane Database of Systematic Reviews is a
collection of evidence-based reviews produced by the
Cochrane Library, an international nonprofit organization.
The reviews summarize the results of clinical trials
on health care interventions. Summaries are free;
full-text reviews are by subscription only.
Web site: cochrane.org/reviews
NCCAM has provided this material for your information. It is not intended to substitute for the medical expertise and advice of your primary health care provider. We encourage you to discuss any decisions about treatment or care with your health care provider. The mention of any product, service, or therapy is not an endorsement by NCCAM.