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HF100 NINTH ENGROSSMENT REVISOR BD 1-10100-9 <br />127.1 (b) The office may by rule establish alternative labeling requirements for lower -potency <br />127.2 edible products that are imported into the state provided that those requirements provide <br />127.3 consumers with information that is substantially similar to the information described in <br />127.4 paragraph (a). <br />127.5 Subd. 4. Additional content of label; medical cannabis flower and medical <br />127.6 cannabinoid products. In addition to the applicable requirements for labeling under <br />127.7 subdivision 2 or 3, all medical cannabis flower and medical cannabinoid products must <br />127.9 include at least the following information on the label affixed to the packaging or container <br />127.9 of the medical cannabis flower or medical cannabinoid product: <br />127.10 (1) the patient's name and date of birth; <br />127.11 (2) the name and date of birth of the patient's registered designated caregiver or, if listed <br />127.12 on the registry verification, the name of the patient's parent, legal guardian, or spouse, if <br />127.13 applicable; and <br />127.14 (3) the patient's registry identification number. <br />127.15 Subd. 5. Content of label; hemp -derived topical products. (a) All hemp -derived topical <br />127.16 products sold to customers must have affixed to the packaging or container of the product <br />127.17 a label that contains at least the following information: <br />127.18 (1) the manufacturer name, location, phone number, and website; <br />127.19 (2) the name and address of the independent, accredited laboratory used by the <br />127.20 manufacturer to test the product; <br />127.21 (3) the net weight or volume of the product in the package or container; <br />127.22 (4) the type of topical product; <br />127.23 (5) the amount or percentage of cannabidiol, cannabigerol, or any other cannabinoid, <br />127.24 derivative, or extract of hemp, per serving and in total; <br />127.25 (6) a list of ingredients; <br />127.26 (7) a statement that the product does not claim to diagnose, treat, cure, or prevent any <br />127.27 disease and that the product has not been evaluated or approved by the United States Food <br />127.28 and Drug Administration, unless the product has been so approved; and <br />127.29 (8) anv other statements or information reauired by the office. <br />127.30 (b) The information required in paragraph (a), clauses (1), (2), and (5), may be provided <br />127.31 through the use of a scannable barcode or matrix barcode that links to a page on a website <br />Article 1 Sec. 63. 127 <br />