Sec. 1. As used in this chapter, "over the counter drug" means a personal care product that contains a label that:
(1) identifies the product as a drug as required by 21 CFR 201.66; and
(2) includes:
(A) a drug facts panel; or
(B) a statement of active ingredients and a list of the ingredients contained in the personal care product.
As added by P.L.21-2015, SEC.5.
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