Read below or choose another question.
Here is some official FDA information on this:
FDA has limited resources to analyze the composition of food products, including dietary supplements. So, FDA focuses first on public health emergencies and products that may have caused injury or illness. Then products thought to be fraudulent or in violation of the law are analyzed. FDA uses the remaining funds for routine monitoring of products pulled from store shelves. FDA does not analyze supplement products before they are sold to consumers. The manufacturer is responsible for ensuring that the ingredient list is accurate and that the ingredients are safe. They are also required to make sure that the content matches the amount declared on the label.
FDA does not have adequate resources to analyze dietary products sent by
consumers who want to know their content. Instead, consumers may contact the
manufacturer or a commercial laboratory.
Manufacturers can also put FDA-approved "health claims" on a
product label. Health
claims describe the connection between a nutrient or food substance and a
disease or health-related condition. Claims about these diet/disease
relationships can appear on the label if the content of the product meets the
FDA requirements and if the claim is one of the approved health claims.
Manufacturers do not need FDA approval to sell their supplement products. This means that FDA does not keep a list of manufacturers or products on the market. If you want more specific information than the label tells you about the products, you may contact the manufacturer directly.
Office of Special Nutritionals, May 1997; Updated April 1999
For more recent information on Dietary Supplements
See http://www.cfsan.fda.gov/~dms/supplmnt.html
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