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fda.gov
Dietary Supplement Continuing Medical Education Program
The FDA in collaboration with the American Medical Association (AMA) has developed an education program to help physicians and other healthcare professionals understand how dietary supplements are regulated in the United States and provide information to patients about their benefits and risks.
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For years, we’ve wrapped our supplements in foil before flying. 🛫 Sounds a little odd, but here’s why it actually makes sense… 🧪 Airport scanners (especially for carry-ons) use radiation to detect what’s inside your bag. But that same radiation can affect the molecular structure of what it touches — including supplements. ⚠️ Radiation can: • Accelerate oxidative reactions • Break down nutrient potency • Degrade sensitive ingredients 💊 Vitamins like A, B-complex, C, and folate are especially v
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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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