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Federal Register / Vol. 86, No. 172 / Thursday, September 9, 2021 / Proposed Rules regulatory action under Executive Order 12866; 2 is not a significant rule under Department of Transportation DOT Regulatory Policies and Procedures 44 FR 11034;
February 26, 1979; and 3 does not warrant preparation of a regulatory evaluation as the anticipated impact is so minimal. Since this is a routine matter that will only affect air traffic procedures and air navigation, it is certified that this proposed rule, when promulgated, will not have a significant economic impact on a substantial number of small entities under the criteria of the Regulatory Flexibility Act.
Environmental Review This proposal will be subject to an environmental analysis in accordance with FAA Order 1050.1F,

FR Doc. 202119321 Filed 9821; 8:45 am BILLING CODE 491013P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration 21 CFR Part 73
Docket No. FDA2021C0925

Fermentalg; Filing of Color Additive Petition lotter on DSK11XQN23PROD with PROPOSALS1

ACTION:

Food and Drug Administration,
Notification of petition.

The Food and Drug Administration FDA or we is announcing that we have filed a petition, submitted by Fermentalg, proposing that the color additive
SUMMARY:

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List of Subjects in 14 CFR Part 71

71.1

Airspace, Incorporation by reference, Navigation air.

The Proposed Amendment In consideration of the foregoing, the Federal Aviation Administration proposes to amend 14 CFR part 71 as follows:
PART 71DESIGNATION OF CLASS A, B, C, D, AND E AIRSPACE AREAS; AIR
TRAFFIC SERVICE ROUTES; AND
REPORTING POINTS

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HHS.

Authority: 49 U.S.C. 106f, 106g; 40103, 40113, 40120; E.O. 10854, 24 FR 9565, 3 CFR, 19591963 Comp., p. 389.
Amended
2. The incorporation by reference in 14 CFR 71.1 of FAA Order 7400.11E, Airspace Designations and Reporting Points, dated July 21, 2020, and effective September 15, 2020, is amended as follows:

Paragraph 2006 United States Area Navigation Routes.

Q73 MOMAR, CA to CORDU, ID
Amended
1. The authority citation for part 71
continues to read as follows:

Issued in Washington, DC, on August 30, 2021.
George Gonzalez, Acting Manager, Rules and Regulations Group.

AGENCY:

Environmental Impacts: Policies and Procedures prior to any FAA final regulatory action.

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regulations be amended to provide for the safe use of blue Galdieria extract, derived from unicellular red algae Galdieria sulphuraria, as a color additive in various food categories at levels consistent with good manufacturing practice.
DATES: The color additive petition was filed on July 27, 2021.
ADDRESSES: For access to the docket to read background documents or comments received, go to https
www.regulations.gov and insert the docket number found in brackets in the heading of this document into the Search box and follow the prompts, and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Stephanie A. Hice, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, 3013481740.
SUPPLEMENTARY INFORMATION: Under section 721d1 the Federal Food, Drug, and Cosmetic Act 21 U.S.C.
379ed1, we are giving notice that we have filed a color additive petition CAP
1C0320, submitted by Fermentalg, 4

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Rue Riviere, 33500 Libourne, France.
The petition proposes to amend the color additive regulations in part 73 21
CFR 73, Listing of Color Additives Exempt from Certification, to provide for the safe use of blue Galdieria extract as a color additive at levels consistent with good manufacturing practice in: 1
Beverages and beverage bases, nonalcoholic; 2 breakfast cereals; 3
chewing gum; 4 confections and frostings; 5 dairy product analogs; 6
frozen dairy desserts and mixes; 7 fruit and water ices; 8 gelatins, puddings, and fillings; 9 hard candy and cough drops; 10 milk products; 11
processed fruits and fruit juices; 12
processed vegetables and vegetable juices; and 13 soft candy.
The petitioner has claimed that this action is categorically excluded under 21 CFR 25.32r because the substance occurs naturally in the environment, and the proposed action does not alter significantly the concentration or distribution of the substance, its metabolites, or degradation products in the environment. In addition, the petitioner has stated that, to their knowledge, no extraordinary
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