Industry Self-Regulation for Dietary Supplements

CHPA members agree voluntarily to take appropriate steps to assure that the following raw materials have not been substituted in whole or in part with known toxic adulterants,

With the exception of certain products, CHPA members agree voluntarily that any product that contains as an ingredient any of the herbs listed below shall include the following information on its label.

CHPA members agree voluntarily to refrain from trade in wild-harvested lady’s slippers.

This document serves as a voluntary guideline to assist manufacturers of dietary supplements with compliance with the dietary supplement current good manufacturing practice (cGMP) requirements of the US FDA 21 CFR §111.

To address the growing need for more information on dietary supplements available in the market, the Office of Dietary Supplements at the National Institutes of Health has developed the Dietary Supplement Label Database. This valuable resource compiles comprehensive information obtained from the labels of dietary supplement products sold in the United States.