General Mills, Inc.; Filing of Food Additive Petition, 21675 [2021-08235]

Download as PDF Federal Register / Vol. 86, No. 77 / Friday, April 23, 2021 / Proposed Rules ‘‘Environmental Impacts: Policies and Procedures’’ prior to any FAA final regulatory action. List of Subjects in 14 CFR Part 71 Airspace, Incorporation by reference, Navigation (air). The Proposed Amendment Accordingly, pursuant to the authority delegated to me, the Federal Aviation Administration proposes to amend 14 CFR part 71 as follows: PART 71—DESIGNATION OF CLASS A, B, C, D, AND E AIRSPACE AREAS; AIR TRAFFIC SERVICE ROUTES; AND REPORTING POINTS 1. The authority citation for 14 CFR part 71 continues to read as follows: ■ Authority: 49 U.S.C. 106(f), 106(g), 40103, 40113, 40120; E.O. 10854, 24 FR 9565, 3 CFR, 1959–1963 Comp., p. 389. § 71.1 [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 6006 Airspace Areas. En Route Domestic * * * * ANM ID E6 * Mountain Home, ID khammond on DSKJM1Z7X2PROD with PROPOSALS That airspace extending upward from 1,200 feet above the surface within an area beginning at Lat. 43°05′36″ N, long. 114°51′26″ W; to Lat. 42°26′27″ N, long. 114°57′44″ W; to Lat. 42°25′53″ N, long. 116°03′43″ W; to Lat. 43°07′42″ N, long. 116°44′08″ W; to Lat. 44°03′18″ N, long. 117°05′05″ W; to Lat. 44°15′42″ N, long. 116°19′34″ W; to Lat. 44°03′41″ N, long. 116°12′15″ W; to Lat. 43°58′04″ N, long. 115°51′09″ W; to Lat. 43°47′52″ N, long. 115°41′21″ W; to Lat. 43°30′14″ N, long. 115°36′38″ W; to Lat. 43°17′24″ N, long. 115°41′05″ W; to Lat. 43°03′38″ N, long. 115°19′32″ W; then to the point of beginning. Issued in Des Moines, Washington, on April 19, 2021. B.G. Chew, Acting Group Manager, Operations Support Group, Western Service Center. [FR Doc. 2021–08445 Filed 4–22–21; 8:45 am] BILLING CODE 4910–13–P VerDate Sep<11>2014 16:19 Apr 22, 2021 Jkt 253001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 172 [Docket No. FDA–2021–F–0366] General Mills, Inc.; Filing of Food Additive Petition Food and Drug Administration, Department of Health and Human Services (HHS). ACTION: Notification of petition. AGENCY: The Food and Drug Administration (FDA or we) is announcing that we have filed a petition, submitted by General Mills, Inc., proposing that the food additive regulations be amended to provide for the safe use of vitamin D3 as a nutrient supplement in yogurt at a level higher than is currently permitted. DATES: The food additive petition was filed on February 3, 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: Marissa Santos, Center for Food Safety and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., College Park, MD 20740, 240–402–8160. SUPPLEMENTARY INFORMATION: Under section 409(b)(5) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 348(b)(5)), we are giving notice that we have filed a food additive petition (FAP 1A4827), submitted on behalf of General Mills, Inc. by Exponent, 1150 Connecticut Ave. NW, Suite 1100, Washington, DC 20036. The petition proposes to amend the food additive regulations in § 172.380 (21 CFR 172.380) Vitamin D3 to provide for the safe use of vitamin D3 as a nutrient supplement in yogurt at a level higher than what is currently permitted. The petitioner has claimed that this action is categorically excluded under 21 CFR 25.32(k) because the substance is intended to remain in food through ingestion by consumers and is not intended to replace macronutrients in food. In addition, the petitioner has stated that, to their knowledge, no extraordinary circumstances exist that would warrant at least an environmental assessment (see 21 CFR 25.21). If FDA 21675 determines a categorical exclusion applies, neither an environmental assessment nor an environmental impact statement is required. If FDA determines a categorical exclusion does not apply, we will request an environmental assessment and make it available for public inspection. Dated: April 16, 2021. Lauren K. Roth, Acting Principal Associate Commissioner for Policy. [FR Doc. 2021–08235 Filed 4–22–21; 8:45 am] BILLING CODE 4164–01–P SUMMARY: PO 00000 Frm 00009 Fmt 4702 Sfmt 4702 POSTAL SERVICE 39 CFR Part 121 Service Standards for MarketDominant Mail Products Postal ServiceTM. Proposed rule. AGENCY: ACTION: The Postal Service seeks public comment on proposed revisions to the service standards for marketdominant mail products. The Postal Service proposes to apply a two-day service standard to intra-Sectional Center Facility (SCF) First-Class Mail where the SCF is both the origin and destination Processing & Distribution Center or Facility (P&DC/F), and to intra-SCF and inter-SCF First-Class Mail if the combined drive time between the origin P&DC/F, destination Area Distribution Center (ADC), and destination SCF is 3 hours or less. For inter-SCF First-Class Mail within the 48 contiguous states (which include, for purposes of these standards, the District of Columbia) where the combined drive time between the origin P&DC/F, destination ADC, and destination SCF is more than 3 hours, but does not exceed 20 hours, the Postal Service proposes a three-day service standard; the same standard would apply for intra-SCF First-Class Mail if the combined drive time exceeds 3 hours and the SCF is not the origin P&DC/F. The Postal Service proposes a four-day service standard for inter-SCF First-Class Mail within the 48 contiguous states where the combined drive time between the origin P&DC/F, destination ADC, and destination SCF is more than 20 hours, but does not exceed 41 hours; and for certain First-Class Mail originating from and/or destined to certain portions of the non-contiguous states and territories. A five-day service standard would apply in the 48 contiguous states if the combined drive time between the origin P&DC/F, destination ADC, and destination SCF exceeds 41 hours, and also for other SUMMARY: E:\FR\FM\23APP1.SGM 23APP1

Agencies

[Federal Register Volume 86, Number 77 (Friday, April 23, 2021)]
[Proposed Rules]
[Page 21675]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-08235]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 172

[Docket No. FDA-2021-F-0366]


General Mills, Inc.; Filing of Food Additive Petition

AGENCY: Food and Drug Administration, Department of Health and Human 
Services (HHS).

ACTION: Notification of petition.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA or we) is announcing 
that we have filed a petition, submitted by General Mills, Inc., 
proposing that the food additive regulations be amended to provide for 
the safe use of vitamin D3 as a nutrient supplement in 
yogurt at a level higher than is currently permitted.

DATES: The food additive petition was filed on February 3, 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: Marissa Santos, Center for Food Safety 
and Applied Nutrition, Food and Drug Administration, 5001 Campus Dr., 
College Park, MD 20740, 240-402-8160.

SUPPLEMENTARY INFORMATION: Under section 409(b)(5) of the Federal Food, 
Drug, and Cosmetic Act (21 U.S.C. 348(b)(5)), we are giving notice that 
we have filed a food additive petition (FAP 1A4827), submitted on 
behalf of General Mills, Inc. by Exponent, 1150 Connecticut Ave. NW, 
Suite 1100, Washington, DC 20036. The petition proposes to amend the 
food additive regulations in Sec.  172.380 (21 CFR 172.380) Vitamin D3 
to provide for the safe use of vitamin D3 as a nutrient 
supplement in yogurt at a level higher than what is currently 
permitted.
    The petitioner has claimed that this action is categorically 
excluded under 21 CFR 25.32(k) because the substance is intended to 
remain in food through ingestion by consumers and is not intended to 
replace macronutrients in food. In addition, the petitioner has stated 
that, to their knowledge, no extraordinary circumstances exist that 
would warrant at least an environmental assessment (see 21 CFR 25.21). 
If FDA determines a categorical exclusion applies, neither an 
environmental assessment nor an environmental impact statement is 
required. If FDA determines a categorical exclusion does not apply, we 
will request an environmental assessment and make it available for 
public inspection.

    Dated: April 16, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2021-08235 Filed 4-22-21; 8:45 am]
BILLING CODE 4164-01-P
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