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Federal Register / Vol. 86, No. 168 / Thursday, September 2, 2021 / Rules and Regulations
b2 of this section, this date will be extended accordingly. If FNS
determines that the report in the first sentence of this paragraph b4 does not sufficiently justify the cases pending status, the case shall be considered overdue. Depending upon the number of overdue cases, FNS may find the State agencys QC system to be inefficient or ineffective and suspend and/or disallow the State agencys Federal share of administrative funds in accordance with the provisions of 276.4.

Cynthia Long, Acting Administrator, Food and Nutrition Service.
FR Doc. 202118743 Filed 9121; 8:45 am BILLING CODE 341030P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration 21 CFR Part 73
Docket No. FDA2018C4117

Listing of Color Additives Exempt From Certification; Butterfly Pea Flower Extract AGENCY:

Food and Drug Administration,
HHS.
ACTION:

Final rule.

The Food and Drug Administration FDA or we is amending the color additive regulations to provide for the safe use of an aqueous extract of butterfly pea flower Clitoria ternatea as a color additive in various food categories at levels consistent with good manufacturing practice. We are taking this action in response to a color additive petition CAP submitted by Exponent, Inc., on behalf of Sensient Colors, LLC Sensient.
DATES: This rule is effective October 5, 2021. See section X for further information on the filing of objections.
Submit either electronic or written objections and requests for a hearing on the final rule by October 4, 2021.
ADDRESSES: You may submit objections and requests for a hearing as follows.
Please note that late, untimely filed objections will not be considered.
Electronic objections must be submitted on or before October 4, 2021. The https www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of October 4, 2021. Objections received by mail/hand delivery/courier for
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written/paper submissions will be considered timely if they are postmarked or the delivery service acceptance receipt is on or before that date.
Electronic Submissions Submit electronic objections in the following way:
Federal eRulemaking Portal:
https www.regulations.gov. Follow the instructions for submitting comments.
Objections submitted electronically, including attachments, to https
www.regulations.gov will be posted to the docket unchanged. Because your objection will be made public, you are solely responsible for ensuring that your objection does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone elses Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your objection, that information will be posted on https www.regulations.gov.
If you want to submit an objection with confidential information that you do not wish to be made available to the public, submit the objection as a written/paper submission and in the manner detailed see Written/Paper Submissions and Instructions.
Written/Paper Submissions Submit written/paper submissions as follows:
Mail/Hand Delivery/Courier for written/paper submissions: Dockets Management Staff HFA305, Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper objections submitted to the Dockets Management Staff, FDA will post your objection, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in Instructions.
Instructions: All submissions received must include the Docket No. FDA
2018C4117 for Listing of Color Additives Exempt From Certification;
Butterfly Pea Flower Extract. Received objections, those filed in a timely manner see ADDRESSES, will be placed in the docket and, except for those submitted as Confidential Submissions, publicly viewable at https www.regulations.gov or at the Dockets Management Staff between 9
a.m. and 4 p.m., Monday through Friday, 2404027500.
Confidential SubmissionsTo submit an objection with confidential
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information that you do not wish to be made publicly available, submit your objections only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION. We will review this copy, including the claimed confidential information, in our consideration of comments. The second copy, which will have the claimed confidential information redacted/
blacked out, will be available for public viewing and posted on https
www.regulations.gov. Submit both copies to the Dockets Management Staff.
If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as confidential. Any information marked as confidential will not be disclosed except in accordance with 21 CFR 10.20
and other applicable disclosure law. For more information about FDAs posting of comments to public dockets, see 80
FR 56469, September 18, 2015, or access the information at: https
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or the electronic and written/paper 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, 2404027500.
FOR FURTHER INFORMATION CONTACT:
Stephen DiFranco, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., College Park, MD 207403835, 240
4022710.
SUPPLEMENTARY INFORMATION:
I. Introduction In a notification published in the Federal Register of November 13, 2018
83 FR 56258, we announced that we filed a color additive petition CAP
8C0313 submitted by Sensient Colors, LLC, c/o Exponent, Inc., 1150
Connecticut Avenue NW, Suite 1100, Washington, DC 20036. The petition proposed to amend the color additive regulations in part 73 21 CFR part 73, Listing of Color Additives Exempt from Certification, to provide for the safe use of an aqueous extract of butterfly pea flower Clitoria ternatea as a color
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