Dietary Supplements

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Informed Consumer Decision Making

The following information on botanical ingredients should be included in either a bulk botanical raw material specification sheet (for business-to-business transactions) or finished product labeling (when selling directly to consumers).

Advertising and marketing of dietary supplements are regulated by the FDA, the FTC, and other governmental organizations. Products must be deemed safe prior to marketing and advertisement claims must be substantiated.

Product Safety & Integrity

Consumer Healthcare Products Association members agree voluntarily to the following provisions pertaining to pyrrolizidine alkaloids.

Product Safety & Integrity

CHPA members agree voluntarily to market products containing kava with the following dosage and labeling.

Informed Consumer Decision Making

Members of the Consumer Healthcare Products Association who market dietary supplements containing St. John's wort initiated a voluntary labeling program on April 2, 2000.

Transparency

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.

CHPA's member-only weekly report from our State & Local Government Affairs team, reporting on recent legislative activity around the country affecting our industry.

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The Health in Hand Foundationleads influential, innovative educational initiatives that address specific areas where consumers need guidance and support.

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