Over-the-counter drug definition

Over-the-counter drug means a drug that contains a label
Over-the-counter drug means a drug that contains a label that identifies the product as a drug as required by 21 C.F.R., Section 201.66. The over-the-counter-drug label includes:
Over-the-counter drug means a drug that contains a label that identifies the product as a drug as

More Definitions of Over-the-counter drug

Over-the-counter drug means a drug that is a personal care product that contains a label that identifies the product as a drug as required by 21 Code of Federal Regulations, Section 201.66 (2014). Such a label includes but is not limited to a drug facts panel or a statement of the active ingredients with a list of those ingredients contained in the base compound, substance or preparation.[PL 2015, c. 4, §1 (NEW).]
Over-the-counter drug means a drug that is not required by federal law to bear the statement "Caution: Federal law prohibits dispensing without prescription."
Over-the-counter drug means a drug that contains a label that identifies the product as a drug as required by 21 C.F.R. § 201.66. The over-the-counter drug label includes: (1) A drug facts panel; or (2) a statement of the active ingredients with a list of those ingredients contained in the compound, substance or preparation. Over-the-counter drugs do not include grooming and hygiene products such as soaps, cleaning solutions, shampoo, toothpaste, antiperspirants and sun tan lotions and screens.
Over-the-counter drug means a drug that contains a label that identifies the product as a drug 4 as required by 21 C.F.R. § 201.66. A member state may exclude “grooming and hygiene 5 products” from this definition. The “over-the-counter-drug” label includes:
Over-the-counter drug means a drug that contains a label that identifies the
Over-the-counter drug means a drug that may be sold without a prescription and which is prescribed by a physician (or other persons authorized to prescribe such drugs under State law).
Over-the-counter drug means a drug that contains a label that identifies the product as a drug as required by 21 C.F.R. 201.66, and the label includes either a "Drug Facts" panel or a statement of the active ingredients with a list of those ingredients contained in the drug.