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Bill > SB066


CO SB066

CO SB066
Regulation of Compounded Weight-Loss Medication


summary

Introduced
01/28/2026
In Committee
01/28/2026
Crossed Over
Passed
Dead

Introduced Session

2026 Regular Session

Bill Summary

The bill establishes regulations for the sale, transfer, or distribution of compounded weight-loss medications, which are custom-made medications that, unlike mass-produced medications, are not subject to approval by the federal food and drug administration (FDA). A person may not sell, transfer, or distribute a compounded weight-loss medication unless the person confirms that the medication: ! Is made from bulk drug substances and drugs that are approved by the FDA when such approval is required; ! Was manufactured in compliance with FDA processes; ! Contains bulk drug substances that are pharmaceutical grade and are accompanied by a certificate of analysis containing information that is material to the safety and efficacy of the bulk drug substances; ! Was manufactured at a facility that is registered with the FDA and passed an FDA inspection within the previous 2 years; and ! Is verified for purity and accurate dosage. Labels for compounded weight-loss medications must list all active and inactive ingredients, the quantity of those ingredients, and the ingredients' country of origin. There must also be a warning on the label stating that the compounded weight-loss medication has not been FDA-approved, has inadequate evidence of safety or efficacy, and has known and unknown side effects. A person must also provide certain disclosures to a patient when prescribing compounded weight-loss medications. The bill prohibits the use of false or misleading claims, including unsubstantiated claims, when advertising or promoting compounded weight-loss medications. A person that sells, transfers, or distributes compounded weight-lost medication must keep records related to the compounded weight-loss medication for at least 2 years after the date of expiration of the compounded weight-loss medication and make those records available for inspection by the state board of pharmacy. The state board of pharmacy may issue fines of up to $1,000 per dose of compounded weight-loss medications that are sold or distributed in violation of the bill and may revoke a pharmacy or business license for violations. The attorney general has authority to enforce this bill as a deceptive trade practice under the "Colorado Consumer Protection Act".

AI Summary

This bill establishes regulations for compounded weight-loss medications, which are custom-made drugs not approved by the U.S. Food and Drug Administration (FDA). To sell, transfer, or distribute these medications, individuals must ensure they are made from FDA-approved bulk drug substances (also known as active pharmaceutical ingredients) or components of FDA-approved drugs, manufactured according to FDA processes, and come with a certificate of analysis detailing their purity and dosage. The facilities where these medications are made must be registered with and inspected by the FDA within the last two years. Labels must clearly list all ingredients, their quantities, and their country of origin, along with a warning that the medication is not FDA-approved, lacks sufficient evidence of safety and effectiveness, and may have unknown side effects. Patients must also receive disclosures about potential side effects and risks. The bill prohibits false or misleading advertising, requires record-keeping for at least two years, and allows the state board of pharmacy to issue fines of up to $1,000 per dose for violations, with the possibility of revoking licenses. The Attorney General can also enforce these provisions as deceptive trade practices under the Colorado Consumer Protection Act.

Committee Categories

Health and Social Services

Sponsors (2)

Last Action

Senate Health & Human Services Committee Hearing (13:30:00 3/5/2026 Old Supreme Court) (on 03/05/2026)

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