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Official State Regulation:
C. Packaging and labeling: a manufacturer applicant shall submit a description and sample of the opaque, child-resistant packaging of the concentrate or cannabis-derived product that the manufacturer shall utilize, including a label that shall contain:
- (1) the name of the entity that produced the cannabis and the name of the manufacturer;
- (2) a batch number or code;
- (3) a production date or expiration date, including a “use by” or “freeze by” date for products capable of supporting the growth of infectious, toxigenic, or spoilage microorganisms;
- (4) a description of the number of units of usable cannabis contained within the product;
- (5) instructions for use;
- (6) warnings for use;
- (7) instructions for appropriate storage;
- (8) approved laboratory analysis, including the results of strength and composition within ten percent (10%) of numbers shown on the package;
- (9) the name of the strain, product facts, or a nutrition fact panel, and a statement that the product is for medical use by qualified patients, to be kept away from children, and not for resale; and
- (10) the name of the department-approved testing facility or facilities used for ingredient testing, and the type(s) of testing conducted.