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HHS/FDA RIN: 0910-AJ28 Publication ID: 2026 
Title: ●Product Standards for Electronic Nicotine Delivery Systems 
Abstract:

This rule would establish new product standards under section 907 of the Federal Food, Drug, and Cosmetic Act for electronic nicotine delivery systems (ENDS). Specifically, this rule would establish product standards for ENDS products to provide greater clarity and predictability for industry and stakeholders by describing standards applicants must meet as part of premarket review.

 
Agency: Department of Health and Human Services(HHS)  Priority: Other Significant 
RIN Status: First time published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: No  Unfunded Mandates: Undetermined 
EO 14192 Designation: Regulatory 
CFR Citation: 21 CFR 1100    21 CFR 1105    21 CFR 1107    21 CFR 1114   
Legal Authority: Section 910 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 387j)    Section 910(b)(1)(G) of the FD&C Act    Section 910(c)(4) of the FD&C Act    Section 906(e) of the FD&C Act (21 U.S.C. 387f(e))    Section 901(b) of the FD&C Act (21 U.S.C. 387a(b))   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  07/00/2026 
Regulatory Flexibility Analysis Required: Undetermined  Government Levels Affected: Undetermined 
Federalism: Undetermined 
Included in the Regulatory Plan: No 
International Impacts: This regulatory action will be likely to have international trade and investment effects, or otherwise be of international interest.
RIN Data Printed in the FR: No 
Agency Contact:
May Nelson
Director, Office of Regulations
Department of Health and Human Services
Food and Drug Administration
Center for Tobacco Products, 10903 New Hampshire Avenue, Document Control Center, Building 71, Room G335,
Silver Spring, MD 20993
Phone:877 287-1373
Email: askctp@fda.hhs.gov