Or. Admin. Code § 845-026-0415 - Standards for Approving Industrial Hemp Products That Contain Artificially Derived Cannabinoids
An industrial hemp product that contains an artificially derived cannabinoid may be approved on or after January 1, 2026, if:
(1) The artificially derived cannabinoid:
(a) Is not a controlled substance under OAR
chapter 855, division 80;
(b) Was
manufactured in compliance with applicable laws relating to food
safety;
(c) In the Commission's
judgment, is not impairing or intoxicating at the intended concentration in the
product; and
(d) Has been reported
as a naturally-occurring component of the plant Cannabis family Cannabaceae in
at least three peer-reviewed publications.
(2) The product is not intended for human
inhalation; and
(3) The
manufacturer of the artificially derived cannabinoid:
(a) Has made a "Generally Recognized as Safe"
(GRAS) determination for the artificial cannabinoid;
(b) Has received a Food and Drug
Administration (FDA) letter responding to a "Generally Recognized as Safe"
(GRAS) notice for the artificially derived cannabinoid manufactured by the same
method that the manufacturer uses, affirming that FDA has no questions about
the notice; or
(c) Has received an
FDA letter of acknowledgement with no objections in response to a New Dietary
Ingredient notification for the artificially derived cannabinoid manufactured
by the same method that the manufacturer uses.
Notes
Statutory/Other Authority: ORS 475C.017, ORS 571.309 & 2024 OL Ch. 16 Sec. 9
Statutes/Other Implemented: ORS 571.309 & 2024 OL Ch. 16 Sec. 9
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