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Bill > A05852


NY A05852

NY A05852
Requires manufacturers of kratom products within the state to have a warning label that the product has not been approved by the federal food and drug administration and the products' side effects; prohibits labeling of kratom products as all natural.


summary

Introduced
02/24/2025
In Committee
06/04/2025
Crossed Over
06/12/2025
Passed
Dead

Introduced Session

2025-2026 General Assembly

Bill Summary

AN ACT to amend the general business law, relating to regulating the sale of kratom products

AI Summary

This bill requires manufacturers of kratom products in New York to include a specific warning label on their packaging starting January 1, 2026. The warning must be in at least 12-point type and a contrasting color, clearly stating that the product has not been approved by the FDA and listing potential side effects including nausea, agitation, hallucinations, breathing difficulties, liver damage, and potential death. The bill also prohibits kratom manufacturers from advertising or labeling their products as "all natural," which is defined as a product containing no artificial ingredients or added colors and minimally processed. Kratom, derived from a Southeast Asian tree, is an herbal supplement that will now be subject to these labeling requirements. Manufacturers who violate these regulations will face civil penalties, with a first violation resulting in a fine of up to $500 and subsequent violations incurring fines of up to $1,000. The law will go into effect one year after its passage, giving manufacturers time to adjust their packaging and marketing practices.

Committee Categories

Business and Industry, Housing and Urban Affairs

Sponsors (8)

Last Action

RETURNED TO ASSEMBLY (on 06/12/2025)

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