15.03.300 Product Package Labelling/Safety Inserts

(a) The dispensing facility shall affix to the approved medical marijuana product package a patient specific dispensing label approved by the Authority, that is easily readable, and firmly affixed and includes:

(1) The name and registry identification number of the certified patient and designated caregiver, if any;

(2) The certifying practitioner's name;

(3) The dispensing facility name, address and phone number;

(4) The dosing and administration instructions;

(5) The quantity and date dispensed;

(6) Any recommendation or limitation by the practitioner as to the use of medical marijuana; and

(7) The expiration date of the product once opened;

(b) The dispensing facility shall place the approved medical marijuana product in a plain outer package when dispensing to the patient or designated caregiver.

(c) The dispensing facility shall ensure that each patient receives approved medical marijuana product from no more than two distinct lots for any 30-day supply dispensed.

(d) The dispensing facility shall include with each product package dispensed to a patient, an Authority approved package safety insert. Information provided shall include but not be limited to:

(1) The medical marijuana product and brand;

(2) A list of any excipients used;

(3) A warning if there is any potential for allergens in the medical marijuana product; 4. Contraindications;

(4) More specific dosage directions and instructions for administration;

(5) Warning of adverse effects and/or any potential dangers stemming from the use of medical marijuana;

(6) Instructions for reporting adverse effects as may be determined by the Authority;

(7) A warning about driving, operation of mechanical equipment, child care or making important decisions while under the influence of medical marijuana;

(8) Information on tolerance, dependence and withdrawal and substance abuse, how to recognize what may be problematic usage of medical marijuana and obtain appropriate services or treatment;

(9) Advice on how to keep the medical marijuana product secure;

(10) Language stating that the certified patient may not distribute any medical marijuana product to anyone else;

(11) Language stating that unwanted, excess, or contaminated medical marijuana product must be disposed of according to Subchapter 21 of Ordinance; and

(12) Language stating that "this product has not been analyzed by the FDA. There is limited information on the side effects of using this product and there may be associated health risks."