This section was included in the new draft rules document on the DOR site:
Regulation 43.3-904. Product Labeling, Substitution, Sampling and Analysis.
A. No licensee, for the sale of medical marijuana shall sell, transfer or give away any medical marijuana that does not contain a label with a list of all chemical additives, including but not limited to nonorganic pesticides, herbicides, and fertilizers that were used in its cultivation and production.
B. In addition, all labels shall include: (1) the license number of the manufacturer, grower, or center; (2) the date of manufacturer, harvest or sale; (3) strains and license numbers where obtained; and (4) the patient registry number of the purchaser.
All “edibles” shall also contain the following statement:
“This product is infused with medical marijuana and was produced without regulatory oversight for health, safety or efficacy and there may be health risks associated with the consumption of the product.”
C. All licensees for the sale of medical marijuana shall, upon request of the MED or any of its officers, make available to the person so requesting a sufficient quantity of such medical marijuana to enable sampling or analysis thereof. The licensee shall be notified of the results of the sampling or analysis without delay.
So, it looks like you can list non organic additives by name instead of chemical list. Every label is going to have to have the patient's number on it. That will suck a little for us because we only sell pre packaged. Maybe we can print a supplemental label or something.
They are making this a huge pain in the ass, but what hasn't been so far :)