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➡️ Under the Dietary Supplement Health and Education Act (DSHEA) of 1994, the FDA does not require pre-market approval, safety testing, or effectiveness proof before supplements hit the market. Literally, manufacturers are largely responsible for ensuring their own products are safe and accurately labeled. This lack of regulations has led to persistent issues like mislabeling. Such as, products containing little or none of the advertised ingredients, contamination with heavy metals, pesticides,

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CHAPTER 7 DIETARY SUPPLEMENTS - SlideServe