Or. Admin. Code § 845-025-7100 - Cannabinoid Concentrate and Extract Labeling Requirements

Prior to a cannabinoid concentrate or extract being sold or transferred to a consumer, patient or designated primary caregiver the container holding the concentrate or extract must have a label that has the following information:

(1) Processor's business or trade name and license number;

(2) Business or trade name of licensee that packaged the product, if different from the processor;

(3) UID number;

(4) Product identity that correctly identifies the item as either a concentrate or extract;

(5) Date the concentrate or extract 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) Activation time, expressed in words or through a pictogram;

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

(11) Universal symbol;

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

(13) For cannabinoid concentrates and extracts 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.

(14) For medical grade cannabinoid concentrates and extracts 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.

Notes

Or. Admin. Code § 845-025-7100

OLCC 6-2018, adopt filed 05/23/2018, effective 6/1/2018; OLCC 152-2022, minor correction filed 03/25/2022, effective 3/25/2022

Statutory/Other Authority: ORS 475C.604

Statutes/Other Implemented: ORS 475C.604