15.03.260 Product Labelling

(a) Each approved medical marijuana product shall be affixed with a product label. Medical marijuana product labels shall be approved by the Authority prior to use. Each product label shall be applied at the manufacturing facility, be easily readable, firmly affixed and include:

(1) The name, address and registration number of the registered entity;

(2) The medical marijuana product form and brand designation;

(3) The single dose THC and CBD content for the product set forth in milligrams (mg);

(4) The medical marijuana product lot unique identifier (lot number or bar code);

(5) The quantity included in the package;

(6) The date packaged;

(7) The date of expiration of the unopened product, based on stability studies in accordance with this Subchapter, or a tentative expiration date approved by the Authority;

(8) The proper storage conditions;

(9) language stating:

(A) "Medical marijuana products must be kept in the original container in which they were dispensed and removed from the original container only when ready for use by the certified patient";

(B) "Keep secured at all times";

(C) "May not be resold or transferred to another person";

(D) "This product might impair the ability to drive";

(E) "KEEP THIS PRODUCT AWAY FROM CHILDREN (unless medical marijuana product is being given to the child under a practitioner's care"); and

(F) "This product is for medicinal use only. Women should not consume during pregnancy or while breastfeeding except on the advice of the certifying practitioner, and in the case of breastfeeding mothers, including the infant's pediatrician."