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HHS/FDA RIN: 0910-AI53 Publication ID: Spring 2025 
Title: Amendment of Procedural Requirements for Color Additive Petitions 
Abstract:

The Food and Drug Administration (FDA) is proposing to amend procedural requirements for color additive petitions (CAPs). This action, if finalized, would modernize the procedural requirements related to the data requirements, submission procedures, review process, and regulatory timeframes for CAPs. 

 
Agency: Department of Health and Human Services(HHS)  Priority: Substantive, Nonsignificant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Long-Term Actions 
Major: No  Unfunded Mandates: No 
EO 14192 Designation: Deregulatory 
CFR Citation: 21 CFR 70    21 CFR 71   
Legal Authority: 21 U.S.C. 321    21 U.S.C. 371    21 U.S.C. 379e   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  09/00/2026 
Regulatory Flexibility Analysis Required: No  Government Levels Affected: None 
Small Entities Affected: No  Federalism: No 
Included in the Regulatory Plan: No 
RIN Data Printed in the FR: No 
Agency Contact:
Paulette Gaynor
Senior Policy Advisor
Department of Health and Human Services
Food and Drug Administration
Humans Foods Program, 4300 River Road Room 2053 (HFS-255),
College Park, MD 20740-3835
Phone:240 402-1192
Fax:301 436-2965
Email: paulette.gaynor@fda.hhs.gov