Or. Admin. Code § 845-025-7110 - Cannabinoid Tincture and Capsule Labeling Requirements
Prior to a cannabinoid tincture or capsule being sold or transferred to a consumer, patient or designated primary caregiver the container holding the tincture or capsule must have a label that has the following information:
(1) Processor's
business or trade name, place of address and license number;
(2) Business or trade name and place of
address of 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
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 tinctures and capsules 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) "BE CAUTIOUS" in
bold, capital letters, followed by "Cannabinoid products can take up to 2 hours
or more to take effect."
(15) For medical grade cannabinoid tinctures
and capsules 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) "It is illegal to drive a motor vehicle
while under the influence of marijuana."
(c) "BE CAUTIOUS" in bold, capital letters,
followed by "Cannabinoid products can take up to 2 hours or more to take
effect."
Notes
Statutory/Other Authority: ORS 475C.604
Statutes/Other Implemented: ORS 475C.604
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