The federal government regulates dietary supplements through the United States Food and Drug Administration (FDA). The regulations for dietary supplements are not the same as those for prescription or over-the-counter drugs. In general, the regulations for dietary supplements are less strict.
To begin with, a manufacturer does not have to prove the safety and effectiveness of a dietary supplement before it is marketed. A manufacturer is permitted to say that a dietary supplement addresses a nutrient deficiency, supports health, or is linked to a particular body function (such as immunity), if there is research to support the claim. Such a claim must be followed by the words “This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.â€
Also, manufacturers are expected to follow certain good manufacturing practices (GMPs) to ensure that dietary supplements are processed consistently and meet quality standards. Requirements for GMPs went into effect in 2008 for large manufacturers and are being phased in for small manufacturers through 2010.
Once a dietary supplement is on the market, the FDA monitors safety and product information, such as label claims and package inserts. If it finds a product to be unsafe, it can take action against the manufacturer and/or distributor and may issue a warning or require that the product be removed from the marketplace. The Federal Trade Commission (FTC) is responsible for regulating product advertising; it requires that all information be truthful and not misleading.
The federal government has taken legal action against a number of dietary supplement promoters or Web sites that promote or sell dietary supplements because they have made false or deceptive statements about their products or because marketed products have proven to be unsafe.
Which statement is not a detail from the passage?
Correct Answer: A
Rationale: The statement "Promoters of dietary supplements can make any claims that are supported by research" is not a detail from the passage. The passage mentions that manufacturers, not promoters, can make claims supported by research. The primary focus is on the regulations and manufacturing standards for dietary supplements. Choice B is a detail from the passage as it mentions the GMP requirements for large manufacturers going into effect in 2008. Choice C is incorrect as the passage states that FDA regulations for dietary supplements are not the same as those for prescription medications. Choice D is also supported by the passage, emphasizing that consumers should research supplement claims before making a purchase to ensure accuracy and safety.
Nokea