Get Your FREE Subscription to HQ Magazine!
Total Product Expo is the highly-anticipated premier B2B trade show that brings manufacturers, distributors, and independent retailers together under one roof.

Where Does the FDA Stand on CBD?

Want to know where the FDA stands on CBD? Check out “What You Need to Know (And What We’re Working to Find Out) About Products Containing Cannabis or Cannabis-derived Compounds, Including CBD.”

In the update, the FDA reiterates its current views about regulation of cannabis products. While the agency acknowledges the tremendous interest in these products, it stresses that many of its scientific and medicinal properties are still unknown. Importantly, the FDA identifies the following issues of concern:

The effects CBD could cause in the body, such as toxicity to the liver, when someone ingests CBD regularly over a long period of time.

The cumulative exposure to CBD if people access it across a broad range of consumer products.

* The effects of CBD on special populations (e.g., the elderly, children, adolescents, pregnant and lactating women) or types of animals (e.g., species, breed, or class).

* The safety of CBD use in animals (e.g., species, breed, or class), including pets.

* The update also once again stresses FDA’s position that the agency will prioritize public health concerns and take enforcement action against manufacturers of CBD products that make claims to prevent, diagnose, or treat diseases. The Update further notes that FDA is also investigating reports of CBD potentially containing contaminants such as pesticides.

* The FDA is continuing to evaluate the regulatory framework for cannabis products and is currently gathering information through its request to stakeholders to submit to the public docket with a deadline of July 2, 2019. Interested stakeholders are encouraged to submit their views to the FDA docket. 

The agency held a public hearing on May 31, and has a high-level task force working through the various issues. It is expected they will make a recommendation about any possible changes to FDA regulations by late summer.