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HHS/FDA RIN: 0910-AI53 Publication ID: Fall 2020 
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. FDA is proposing to revise the regulations to provide additional transparency, streamline current procedures, ease regulatory burden, and modernize the regulations.  The proposed rule, if finalized, would improve regulatory efficiencies by implementing petition data requirements that are specific to the requested action.

 
Agency: Department of Health and Human Services(HHS)  Priority: Substantive, Nonsignificant 
RIN Status: First time published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: No  Unfunded Mandates: No 
EO 13771 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  08/00/2021 
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:
Annette McCarthy
Consumer Safety Officer
Department of Health and Human Services
Food and Drug Administration
5001 Campus Drive,
College Park, MD 20740
Phone:240 402-1057
Email: annette.mccarthy@fda.hhs.gov