(A) Every medical marijuana strain and every medical marijuana product shall be registered with the department and assigned a product identifier by the state of Ohio board of pharmacy before it may be sold to a dispensary or dispensed to a patient or caregiver. Before a product is eligible for the assignment of a product identifier, in accordance with rules promulgated by the state of Ohio board of pharmacy, the product shall be registered with the department.
(B) Each registration application shall include the proposed label, and any other items deemed necessary by the department or in accordance with rules promulgated by the state of Ohio board of pharmacy. A separate registration is required for each package size and dose of a particular strain or product before the strain or product may be offered for sale. A variation in ingredients shall constitute a new product and require a separate product registration and product identifier.