Dietary Supplements

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Dietary Supplements: What (2013) founds that dietary supplement may be perceived as a harmless stimulant to health. Some of dietary supplement products have demonstrated benefits, many of which we cannot say the same. Unlike what happens with curative drugs, the FDA does not evaluate the safety and effectiveness of dietary supplements, and depending on current medications or health problems we have; "natural" supplements can have risky health effects. This lack of regulation can lead to wildly inconsistent quality and there are no guarantees that the ingredient touted on the label of a bottle will be in the supplement at all. According to federal law, dietary supplements cannot be promoted as effective for the treatment of a disease because that is not proven to be safe and effective. According with Desai, K. (2012) the consumer reports from 2007 …show more content…

This means that: The FDA does not approve dietary supplements before producing or put them on sale, and can only take action against products that are unsafe or products that make false claims after they are on sale. In other words, the FDA cannot even inspect the manufacturing process of the company unless there is reasonable evidence that their products are harming people-and this means that some people need to be hurt before the FDA can step in; if somebody ask me that is a bit late. It is incredible that someone has to be damaged in order that FDA takes action. The dietary supplement manufacturers are responsible for the safety of its products and must meet a series of standards for quality assurance in manufacturing, packaging and labeling of their products. Manufacturers of dietary supplements should also make monitoring for adverse events reported regarding their products and report all serious adverse events to the FDA. The advertising of dietary supplements is regulated by the Federal Trade Commission

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