Here’s what you should know about those CBD beverages and snacks you might see at your local drug store or supermarket.
What is CBD?
In 2019 alone, the FDA sent warning letters to more than 20 companies selling CBD products, demanding that they remove or remedy their various health and medical claims. Despite all this, CBD companies and industry experts don’t expect CBD products to go anywhere.
Are CBD foods and drinks safe?
What’s more, because CBD is currently a relatively unregulated ingredient (other than, you know, the fact that it’s illegal to market), some products make health and medical claims that may not be true and may use ingredients of unknown quality.
19. Can patients gain access to cannabis or cannabis-derived products for medical use through Right to Try?
18. How can patients gain access to cannabis or cannabis-derived products for medical use through expanded access?
15. Can I import or export cannabis-containing or cannabis-derived products?
Research and Expanded Access
1. What are cannabis and marijuana?
A. All ingredients in animal food must be the subject of an approved food additive petition or generally recognized as safe (GRAS) for their intended use in the intended species. If an animal food contains an ingredient that is not the subject of an approved food additive petition or GRAS for its intended use in the intended species, that animal food would be adulterated under section 402(a)(2)(C)(i) of the FD&C Act [21 U.S.C. § 342(a)(2)(C)(i)]. In coordination with state feed control officials, CVM also recognizes ingredients listed in the Official Publication (OP) of the Association of American Feed Control Officials (AAFCO) as being acceptable for use in animal food. At this time, there are no approved food additive petitions or ingredient definitions listed in the AAFCO OP for any substances derived from hemp, and we are unaware of any GRAS conclusions regarding the use of any substances derived from hemp in animal food. Learn more about animal food ingredient submissions here.
A. A cosmetic is defined in 201(i) as “(1) articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to the human body or any part thereof for cleansing, beautifying, promoting attractiveness, or altering the appearance, and (2) articles intended for use as a component of any such articles; except that such term shall not include soap.”
Questions and Answers
20. Does the FDA have concerns about administering a cannabis product to children?
The 2018 Farm Bill, however, explicitly preserved FDA’s authority to regulate products containing cannabis or cannabis-derived compounds under the FD&C Act and section 351 of the Public Health Service Act (PHS Act). FDA treats products containing cannabis or cannabis-derived compounds as it does any other FDA-regulated products — meaning they’re subject to the same authorities and requirements as FDA-regulated products containing any other substance. This is true regardless of whether the cannabis or cannabis-derived compounds are classified as hemp under the 2018 Farm Bill.