Or. Admin. Code § 845-025-7120

Current through Register Vol. 63, No. 10, October 1, 2024

Section 845-025-7120 - Cannabinoid Products Other than Cannabinoid Edibles, Topicals, Tinctures or Capsules.

Prior to a cannabinoid product other than a cannabinoid edible, topical, tincture or capsule being sold or transferred to a consumer, patient or designated primary caregiver, the container holding the product must have a label that has the following information:

(1) Processor's business or trade name, license number, and place of address;

(2) Business or trade name of licensee, license number, and place of address for licensee that packaged the product, if different from the processor;

(3) Product identity;

(4) UID number;

(5) Date the product was made;

(6) Net weight or volume in U.S. customary and metric units;

(7) Serving size and number of servings per container;

(8) Amount, in milligrams, of THC and CBD in each serving and in the container;

(9) List of all ingredients in descending order of predominance by weight or volume used to process the cannabinoid product;

(10) Name of the lab that performed any test and any test analysis date;

(11) Universal symbol;

(12) Activation time expressed in words or through a pictogram;

(13) A statement that reads: "This product is not approved by the FDA to treat, cure, or prevent any disease";

(14) For cannabinoid products for sale to a consumer, warnings that state:

(a) "For use only by adults 21 and older. Keep out of reach of children."

(b) "Do not drive a motor vehicle while under the influence of marijuana."

(c) "DO NOT EAT" in bold, capital letters.

(15) For medical grade cannabinoid products for use by a patient, the medical grade symbol and medical warnings that state:

(a) "For use by OMMP patients only. Keep out of reach of children."

(b) "Do not drive a motor vehicle while under the influence of marijuana."

(c) "DO NOT EAT" in bold, capital letters.

(16) For inhalable cannabinoid products that contain non-cannabis additives:

(a) The product identity must clearly identify that the product contains non-cannabis additives and, in addition to the other requirements of OAR 845-025-7000 through 845-025-7190, must include the words "non-cannabis additive."

(b) In addition to the other ingredients in the inhalable cannabinoid product, for each non-cannabis additive used, the ingredient listing must contain the words "non-cannabis additive" in a manner that clearly distinguishes each additive from any other additives.

(c) All of the ingredients in the non-cannabis additive:

(A) Must match the ingredients identified on the list of ingredients required by OAR 845-025-3265(1);

(B) Must be listed either alphabetically or in descending order of predominance by weight or volume; and

(C) Must be listed on:

(i) The label's ingredient list as sub-ingredients of the ingredient term "non-cannabis additive"; or

(ii) An insert within the product's container that clearly indicates that the ingredients listed are contained within the inhalable cannabinoid product.

Or. Admin. Code § 845-025-7120

OLCC 6-2018, adopt filed 05/23/2018, effective 6/1/2018; OLCC 24-2020, amend filed 12/21/2020, effective 12/22/2020; OLCC 154-2022, minor correction filed 03/25/2022, effective 3/25/2022

Statutory/Other Authority: ORS 475C.604, 475C.233 & 475C.237

Statutes/Other Implemented: ORS 475C.604