New Mexico Register / Volume XXX, Issue 20 / October 29, 2019

 

 

This is an emergency amendment to 7.34.4 NMAC, Section, 14, effective 10/4/2019.

 

7.34.4.14               LABELING OF USABLE CANNABIS:  A non-profit producer shall not sell or otherwise distribute a usable cannabis product that has not been packaged and labeled in accordance with this rule.

A.            The label shall identify:

                [A.]         (1)           the name of the entity that produced the cannabis, and the name of the manufacturer of the cannabis-derived product (as applicable);

                [B.]         (2)           a batch number or code;

                [C.]         (3)           a production date or expiration date, including a “use by” or “freeze by” date for products capable of supporting the growth of infectious, toxigenic, or spoilage microorganisms;

                [D.]         (4)           the number of units of usable cannabis or concentrated cannabis-derived product contained within the product, as identified in department rules for the enrollment of qualified patients;

                [E.]         (5)           for dried, usable cannabis:  the quantity of THC and CBD, which shall be expressed by weight;

                [F.]          (6)           for concentrated cannabis derived product:  the quantity of THC and CBD, which shall be expressed by weight and by percentage of total weight;

                [G.]         (7)           pesticide(s) used in the production of the cannabis or cannabis-derived product;

                [H.]         (8)           instructions for use;

                [I.]           (9)           warnings for use;

                [J.]          (10)         instructions for appropriate storage;

                [K.]         (11)         approved laboratory analysis, including the results of strength and composition within ten percent (10%) of numbers shown on the package;

                [L.]         (12)         the name of the strain, product facts, or a nutrition fact panel, and a statement that the product is for medical use by qualified patients, to be kept away from children, and not for resale;

                [M.]        (13)         whether the batch from which the product was derived was sampled and tested by an approved laboratory; and

                [N.]         (14)         the name of the department approved testing facility used for active ingredient analysis, and quantity of THC and CBD (as applicable).

                B.            Vaporization products label:  All cannabis-derived products that are intended to be consumed by vaporization must additionally include a plainly legible health warning on the label that states in bolded text, “WARNING: Vaping cannabis-derived products containing tetrahydrocannabinol (THC) has been associated with cases of severe lung injury, leading to difficulty breathing, hospitalization, and even death.”

[7.34.4.14 NMAC - N, 2/27/2015; A, 2/29/2016; A/E, 10/4/2019]