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HHS/FDA

RIN: 0910-AI53

Publication ID: Spring 2022

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: Previously published in the Unified Agenda	Agenda Stage of Rulemaking: Proposed Rule Stage
Major: No	Unfunded Mandates: No
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	03/00/2023

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