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 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
Over-the-counter drug means a drug that contains a label that identifies the product as a drug as required by Code of Federal Regulations, title 21, section 201.66. The label must include a "drug facts" panel or 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, regardless of whether they otherwise meet the definition. "Grooming and hygiene products" are soaps, cleaning solutions, shampoo, toothpaste, mouthwash, antiperspirants, and suntan lotions and sunscreens.
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 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 contains a label that identifies the product as a drug 21 as required by 21 C.F.R. § 201.66. A member state may exclude “grooming and hygiene 22 products” from this definition. The “over-the-counter-drug” label includes: