Why Supplement Label Language Matters Supplements are everywhere — in fact, more than half of U.S. adults take at least one. But a new study published in JAMA Network Open highlights a persistent challenge: consumers often interpret common label language as medical promises. Phrases like “supports heart health” or “boosts cognitive function” are intended to […]
Learn More
Regulatory Blind Spots Can Cost You Launching a supplement brand without a clear grasp of regulatory requirements is one of the most common and most damaging mistakes. The FDA closely monitors supplement labeling, claims, and ingredient submissions, and missing these steps can mean costly delays, recalls, or even legal action. New brands often underestimate how […]
Learn More
FDA’s New Dietary Ingredient Notification — What It Means for You The FDA has recently released new educational materials to help manufacturers and distributors navigate the new dietary ingredient notification (NDIN) review process. This process represents the agency’s only chance to evaluate the safety and identity of a new dietary ingredient before it reaches consumers. […]
Learn More