§2429-C. Edible cannabis products health and safety requirements and restrictions
In addition to all other applicable provisions of this chapter, edible cannabis products to be sold or offered for sale in a retail transaction in accordance with this chapter: [PL 2017, c. 452, §18 (NEW); PL 2021, c. 669, §5 (REV).]
1. Cannabinoid content. Must be manufactured in a manner that results in the cannabinoid content within the product being homogeneous throughout the product or throughout each element of the product that has a cannabinoid content;
[PL 2017, c. 452, §18 (NEW).]
2. Cannabis content. Must be manufactured in a manner that results in the amount of cannabis concentrate within the product being homogeneous throughout the product or throughout each element of the product that contains cannabis concentrate;
[PL 2017, c. 452, §18 (NEW); PL 2021, c. 669, §5 (REV).]
3. Shape. May not be manufactured in the distinct shape of a human, animal or fruit;
[PL 2017, c. 452, §18 (NEW).]
4. Additives. May not contain additives that are:
A. Toxic or harmful to human beings; or [PL 2017, c. 452, §18 (NEW).]
B. Specifically designed to make the product appeal particularly to a person under 21 years of age; and [PL 2017, c. 452, §18 (NEW).]
[PL 2017, c. 452, §18 (NEW).]
5. Addition to trademarked food or drink. May not involve the addition of harvested cannabis to a trademarked food or drink product, except when the trademarked product is used as a component of or ingredient in the edible cannabis product and the edible cannabis product is not advertised or described for sale as containing the trademarked product.
[PL 2019, c. 331, §30 (AMD); PL 2021, c. 669, §5 (REV).]
SECTION HISTORY
PL 2017, c. 452, §18 (NEW). PL 2019, c. 331, §30 (AMD). PL 2021, c. 669, §5 (REV).
Structure Maine Revised Statutes
Chapter 558-C: MAINE MEDICAL USE OF CANNABIS ACT
22 §2422-A. Administration and enforcement; rulemaking
22 §2423. Protections for the medical use of marijuana (REPEALED)
22 §2423-A. Authorized conduct for the medical use of cannabis
22 §2423-B. Authorized conduct by a medical provider
22 §2423-C. Authorized conduct
22 §2423-D. Authorized conduct by a visiting qualifying patient
22 §2423-E. Requirements (REPEALED)
22 §2423-F. Cannabis manufacturing facilities
22 §2425. Registry identification cards (REPEALED)
22 §2425-A. Registry identification cards and registration certificates
22 §2427. Affirmative defense and dismissal for medical marijuana (REPEALED)
22 §2428. Registered dispensaries
22 §2429. Enforcement (REPEALED)
22 §2429-A. Packaging and labeling requirements
22 §2429-B. Signs, advertising and marketing
22 §2429-C. Edible cannabis products health and safety requirements and restrictions
22 §2430. Medical Use of Cannabis Fund established
22 §2430-A. Compliance (REPEALED)
22 §2430-B. Admissibility of records
22 §2430-C. Protections for authorized activity
22 §2430-D. Collectives prohibited
22 §2430-E. Possession penalties; fraud penalty
22 §2430-F. Registration suspension or revocation
22 §2430-G. Record keeping; inspections; reporting requirements