SB 1734 Florida Senate · 2025 Regular Session

Florida Kratom Consumer Protection Act

Summary
Florida Kratom Consumer Protection Act; Revising the definition of the term “kratom product”; prohibiting processors from manufacturing, delivering, offering for sale, distributing, or selling finished kratom products that do not meet specified requirements; requiring that kratom products be manufactured by, delivered to, offered for sale by, distributed by, or sold by a processor who holds a certain permit; requiring such processors to be registered with the United States Food and Drug Administration; prohibiting the serving of kratom beverages combined with alcohol, drugs, or other kratom products, etc. APPROPRIATION: $3,711,749
Bill status died 1 of 4 stages cleared
Introduction
Mar 2025
Committee Review
Floor Vote
Governor
Introduced Mar 10, 2025 Last action Jun 16, 2025
Maddy AI version diff · 1 comparison

What changed between versions

S 1734 Filed S 1734 c1 · 8 edits
MODERATE
This bill expanded the Florida Kratom Consumer Protection Act to include new product forms like gummies and liquid dietary supplements, added stricter labeling requirements including age and pregnancy warnings, and tightened laboratory testing standards by requiring Florida-based university labs. The changes aim to increase consumer safety and regulatory oversight of kratom products in the state.
Scope change
The bill's scope expanded to include additional product forms (gummies, liquid dietary supplements) and added new product categories that were previously not explicitly covered under the approved delivery forms.
DEFINITION

Added 'liquid dietary supplement' and 'gummy or food that are not attractive to children' to approved kratom product delivery forms.

REQUIREMENT

Expanded labeling requirements to include warnings about age restrictions (under 21), pregnancy/breastfeeding, and safe consumption limits within 24 hours.

Added container requirements mandating compliance with Poison Prevention Packaging Act and inclusion of graduated measuring devices.

Changed laboratory testing requirements to mandate Florida-based university laboratories accredited under ISO/IEC 17025:2017 standards.

Extended certificate of analysis retention period to minimum of 1 year after product expiration date.

Added requirement for processors to submit adverse health event reports to FDA following federal Food, Drug, and Cosmetic Act guidelines.

ENFORCEMENT

Increased penalties for violations involving synthetic alkaloids from misdemeanor to felony of the third degree.

TIMELINE

Maintained July 1, 2025 effective date for the act.

Floor votes

How they voted

No floor votes recorded yet.
Full legislative history

Actions timeline

Total actions
10
Key actions
3
Committee
4
Mar 26, 2025
Upper · Passed
Now in Appropriations Committee on Agriculture, Environment, and General Government
upper
Mar 26, 2025
Upper · Passed
Pending reference review under Rule 4.7(2) - (Committee Substitute)
upper
Mar 20, 2025
Upper · Passed
On Committee agenda-- Commerce and Tourism, 03/25/25, 8:30 am, 110 Senate Building
upper
Mar 10, 2025
Introduced
Introduced
upper
Mar 7, 2025
Committee
Referred to Commerce and Tourism; Appropriations Committee on Agriculture, Environment, and General Government; Fiscal Policy
upper
1 primary · 1 co-sponsor

Sponsors