By Nancy Glick, Director of Food and Nutrition Policy, seen in Colorado Politics  

“As goes California, so goes the nation” is a phrase reflecting California’s reputation as a bellwether in setting regulations that often become a precedent for national policy.

Now, Colorado can play this role, setting new safety standards that will protect 1.4 million Coloradans with obesity from harm if they take a GLP-1 weight loss drug.

The opportunity at hand is SB066, proposed legislation under consideration in the Colorado state Senate that, if enacted into law, could be a gamechanger for consumers. This is because the bill would put stringent guardrails on the manufacture and sale of unapproved compounded GLP-1 drugs the Food and Drug Administration (FDA) warns could cause serious harm due to dosing errors and reactions to harmful ingredients. Underscoring the potential health consequences for patients,

as of Sept. 9, 2025, the FDA has received 1,424 reports of adverse events associated with compounded GLP-1 drugs, including reports of hundreds of hospitalizations and 23 deaths.

Understanding what brought us to this point is helpful to appreciate the significance of SB066 in solving the problem. Currently, FDA regulates compounded drugs as one-of-a-kind medications modified when a person needs a different form or dosage. This is the primary purpose for a compounded drug, which is why these drugs are not FDA-approved and why the agency exempts licensed compounding pharmacies from meeting rigorous safety standards required for other prescription medicines, such as clinical testing and labeling with risk information.

Yet these exemptions also apply when compounders mass produce modified drugs to fill a supply gap during a shortage, meaning sellers can take advantage of regulatory loopholes to make massive profits. This was the case between 2022 and early 2025 when there was a shortage of the GLP-1 drugs semaglutide and tirzepatide. Because booming consumer demand for GLP-1s was a primary reason for the shortages, it was a gold rush situation for compounders who made full use of regulatory gaps to build a large secondary market for their compounded GLP-1s by advertising the benefits without disclosing the risks.

The shortage also highlighted the problem the active pharmaceutical ingredients (API) used by compounders often come from China, where quality standards vary widely and the API may go uninspected. According to a Brookings Institution report, fewer than one-quarter of Chinese facilities marketing bulk semaglutide have been inspected by the FDA, despite significant shipments to the U.S.

Yet, consumers were not aware of these safety concerns, they believed the advertising claims, and profits soared. Thus, despite FDA announcing the end of the GLP-1 drug shortage in March 2025 and setting May 22 as the last day when compounded versions could be sold, the large-scale production of compounded GLP-1s continues unabated. Moreover, now, the market features “personalized” formulations with added vitamins or microdoses of GLP-1s that have never been evaluated as well as patches, gummies and drops that are not actual GLP-1 products.

The good news is the FDA is starting to remove questionable active ingredients from the GLP-1 market and is cracking down on telehealth companies making false and misleading advertising claims. Similarly, the U.S. Congress is considering legislation to strengthen FDA oversight, close regulatory loopholes and require reforms that will protect consumers from misinformation and inferior products.

Yet states are equal partners with FDA when it comes to compounding practices and can regulate drug compounding to tighten state controls and impose new oversight measures. For this reason, SB066 can be the change agent at the state level that will protect consumers and safeguard patient safety.

Of special importance to the National Consumers League, the bill would prohibit false and misleading advertising of compounded GLP-1s; compel labels that clearly list all ingredients, their quantities, and their country of origin; require a warning the medication is not FDA-approved; and ensure patients receive information about risks and side effects. Additionally, SB066 addresses safety concerns about the source of the API in compounded GLP-1s by setting strict standards for how the ingredients are manufactured, including the facilities where the medications are made must be registered with and inspected by the FDA.

All of these provisions are “must-haves” that will have a meaningful effect for Coloradans and the public at large.

Nancy Glick is director of Food and Nutrition Policy for the National Consumers League, a position she has held since September 2020.