Tag: Fda regulation supplements

According to the National Institutes of Health, over half of U.S. adults use a dietary supplement regularly. However, despite their widespread popularity, many consumers are left wondering: are natural supplements safe? The truth is far more complex than the simple word 'natural' suggests.

According to one industry report, Americans spend upwards of $35 billion per year on supplements, highlighting the scale of the market. With many options available, consumers often wonder if lower-priced store brand supplements offer the same quality and efficacy as their more expensive, well-known counterparts.

According to the Food and Drug Administration (FDA), dietary supplements are regulated as food, not drugs, which creates a critical distinction in how they are brought to market and monitored for safety. The simple question of whether supplements are food or drugs uncovers a complex regulatory landscape that profoundly affects consumers.

Over half of all American adults regularly take a multivitamin, but is it a real vitamin in the same sense as what's found in food? This question leads to a deeper scientific discussion involving how supplements are made, how the body absorbs them, and whether they can genuinely fill nutritional gaps.

According to a survey by The Pew Charitable Trusts, about half of American adults mistakenly believe the FDA reviews or tests all dietary supplements before they are sold. This makes understanding what does USP mean on vitamins crucial for ensuring product quality and safety.