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]