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FDA: Dietary supplements must comply with good manufacturing practices. . .

Good manufacturing practices (eGMP) will ensure that dietary supplements are labeled accurately, are produced in a quality manner, and do not contain impurities or contaminants.

The new FDA regulations cover good practice in all stages of the product's life cycle from manufacturing through packaging and labeling to storage. The dietary supplement industry will also have to report adverse events to the FDA. However, the Consumers Union says the rules do not go far enough. Unlike prescription drugs, dietary supplements do not have to prove they are safe and effective BEFORE consumers can buy them. A Consumers Union spokesperson said that it is still a case of "buyer beware for consumers of dietary supplements because manufacturers are not required to list known health risks for their products, or make sure that they are safe and effective." The FDA regulations will be in effect starting August 24.

Source: Medical News Today

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