N.M. Admin. Code § 20.10.2.13

Current through Register Vol. 35, No. 24, December 23, 2024

Section 20.10.2.13 - HEMP FINISHED PRODUCT LABELING

A. After the effective date of this part and unless otherwise provided, hemp finished products produced for:

(1) human consumption shall meet the applicable labeling requirements of 21 CFR 101 and the New Mexico Food Act; and

(2) absorption by humans shall meet the applicable labeling requirements of 21 CFR 701 and 740.

(3) inhalation by humans shall meet applicable state and federal labeling requirements.

B. In addition to the labeling requirements specified in Subsection A of this section, hemp finished products shall clearly identify on the principle display panel of the label:

(1) CBD content in the package and/or container, labeled in milligrams; and

(2) Total THC content in the package and/or container, labeled in milligrams.

C. In addition to the labeling requirements specified in Subsections A and B of this section, hemp finished products shall include the following statement on the label: "FDA has not evaluated this product for safety, effectiveness, and quality".

D. Unless otherwise approved, statements representing or inferring a hemp finished product contains no THC are prohibited.

E. Hemp facilities shall design, maintain and use a coding system that will identify the date and place of manufacture of each hemp product and shall be clearly visible on the product label or securely affixed to the body of the container.

F. Except as specified in paragraph (1) of Subsection D of 20.10.2.14 NMAC, product concentration and content stated on a hemp finished product label shall not deviate by more than ten percent of what is stated on the label.

G. Hemp finished products shall not contain medical, health, or benefit claims on the label.

N.M. Admin. Code § 20.10.2.13

Adopted by New Mexico Register, Volume XXX, Issue 15, August 13, 2019, eff. 8/1/2019, Amended by New Mexico Register, Volume XXXI, Issue 02, January 28, 2020, eff. 1/28/2020