Are medical marijuana products labeled to indicate their intended use?

In Virginia, medical marijuana products must be labeled in order to indicate their intended use. The Virginia Board of Pharmacy has established regulations requiring manufacturers to identify the medical marijuana product by its brand name, product name, and form. Labels must also include the amount of THC, the active ingredient in marijuana, per serving, the cannabinoid profile, the date of manufacturing, the batch number, the expiration date, the name of the manufacturer, the name of the medical marijuana dispensary, and the quantity of the product. The Virginia Board of Pharmacy also requires medical marijuana products to have certain warnings on their labels. These include warnings that the product is for medical use only, that the product should not be used by those under the age of 18 or those pregnant, and that the product may impair driving and other activities. The labeling of medical marijuana products ensures that users have access to information about these products that is required for safe and effective use. It also helps to protect consumers from any unscrupulous sellers who might otherwise attempt to distribute recreational marijuana in the guise of medical marijuana products.

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Are medical marijuana products labeled to indicate their intended use?

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