Sleek, for the sake of brevity, I have to simply ask, in a CBD isolate-only industry, what would separate CBD food, dietary supplements, and drugs, besides the dosage amount?
1 CBD cookie= Food?
2 CBD cookies= Dietary Supplement?
3 CBD cookies= an FDA Approved Drug?
I don't think this is any way to really regulate anything as I can just eat 3x food to have a drug.
Also, I don't look at the House Bill as something that the FDA has a say in, not only because the FDA does not make legislation, but because the bill would not be necessary at all if congress agreed with the approach the FDA has taken to regulate hemp this past year, which so far has been to just hide behind their conspicuously timed approval of Epidiolex.
No, I see the house bill as a message to the FDA, that if they don't get their butts in gear to regulate, Congress will override them and do their job for them, in a way they wont like.
So, what is it, in your opinion, aside from dosage amount, that would separate the three categories for CBD products, in an isolate only industry?