Tag: Labeling

According to the FDA, a significant number of product recalls are the result of manufacturers' misinterpretations of a product's intended use and indications for use. Understanding **what's the difference between intended use and indications for use?** is therefore not just a matter of semantics but is vital for regulatory compliance, clinical decision-making, and patient safety. Manufacturers, regulators, and healthcare professionals must have a crystal-clear understanding of these distinct concepts.

According to the USDA, products labeled “100% organic” must contain only organically produced ingredients, excluding water and salt, and no other additives. Understanding this definition is the key to discerning whether a product is truly 100% pure organic and free from synthetic chemicals or genetic modifications.