Which agency is responsible for taking action against unsafe supplements after they reach the market?

Question

BlackTom AI · Accepted Answer

To start, we need to identify which agency governs enforcement actions against unsafe supplements after they’re already on the market.
Option 1: Food and Drug Administration (FDA) — This agency is the primary regulator for dietary supplements in the United States after they reach consumers. The FDA oversees labeling, manufacturing practices, and safety concerns, and it can take enforcement actions such as recalls, warnings, or injunctions when a supplement is found to be unsafe or adulterated.
Option 2: U.S. Department of Agriculture (USDA) — The USDA regulates agricultural products, including certain foods and animal feed, but it is not the lead agency for dietary supplement safety in the market. Its focus is more on agriculture and food safety within that domain, not the broad dietary supplement market.
Option 3: National Institutes of Health (NIH) — The NIH funds and conducts medical research and provides health information, but it does not regulate or enforce safety actions against supplements in the market. Its role is primarily scientific research rather than regulatory enforcement.
Option 4: World Health Organization (WHO) — The WHO provides international public health guidance and standards, but it does not take enforcement actions within the United States against consumer products like supplements. Regulation and enforcement in the U.S. are handled by national agencies, not by WHO.
Overall, the correct regulatory body responsible for taking action against unsafe supplements after they reach the market is the FDA, since it oversees post-market safety, labeling, and compliance for dietary supplements. The other agencies play either a broader agricultural/health research role or international guidance and do not directly enforce U.S. post-market supplement safety.

fshn_120_120258_248655 CHAPTER 10 DEFINITION INQUISITION (DI) - 3 TAKES - HIGHEST SCORE COUNTS

Which agency is responsible for taking action against unsafe supplements after they reach the market?

查看解析

登录即可查看完整答案

类似问题

Question at position 7 The FDA has little authority to investigate the contents of supplements until after people get sick from consuming them.TrueFalse

Which of the following products is commonly mistaken as FDA approved but is not?

Question at position 7 The FDA has little authority to investigate the contents of supplements until after people get sick from consuming them.The FDA has little authority to investigate the contents of supplements until after people get sick from consuming them.TrueFalse题目解析

In a consumer society, many adults channel creativity into buying things

Economic stress and unpredictable times have resulted in a booming industry for self-help products

People born without creativity never can develop it

A product has a selling price of $20, a contribution margin ratio of 40% and fixed cost of $120,000. To make a profit of $30,000. The number of units that must be sold is: Type the number without $ and a comma. Eg: 20000

Which of the following statement regarding cost is correct:

更多留学生实用工具

考试浏览器助手

风格化写作助手

论文查重助手

文献引用助手

课堂转译助手

课堂笔记助手

Quiz搜索助手

学校历年真题

智能刷题助手

智能匹配练习

希望你的学习变得更简单