Fermentalg; Filing of Color Additive Petition, 50495-50496 [2021-19405]
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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,
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[FR Doc. 2021–19321 Filed 9–8–21; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 73
[Docket No. FDA–2021–C–0925]
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:
VerDate Sep<11>2014
17:23 Sep 08, 2021
Jkt 253001
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 71—DESIGNATION OF CLASS A,
B, C, D, AND E AIRSPACE AREAS; AIR
TRAFFIC SERVICE ROUTES; AND
REPORTING POINTS
FIX
WP
WP
WP
WP
WP
WP
WP
WP
WP
WP
WP
WP
WP
WP
FIX
*
HHS.
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.
[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.
*
*
*
*
*
Q–73 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.
■
MOMAR, CA
LVELL, CA
BLKWL, CA
ZELMA, CA
KRLIE, CA
HAKMN, NV
LAKRR, NV
GUNTR, AZ
ZAINY, AZ
EEVUN, UT
WINEN, UT
CRITO, NV
BROPH, ID
DERSO, ID
ZATIP, ID
CORDU, ID
*
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48°10′46.41″
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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, 301–348–1740.
SUPPLEMENTARY INFORMATION: Under
section 721(d)(1) the Federal Food,
Drug, and Cosmetic Act (21 U.S.C.
379e(d)(1)), we are giving notice that we
have filed a color additive petition (CAP
1C0320), submitted by Fermentalg, 4
PO 00000
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Rue Rivie`re, 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 25.32(r) 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
E:\FR\FM\09SEP1.SGM
09SEP1
50496
Federal Register / Vol. 86, No. 172 / Thursday, September 9, 2021 / Proposed Rules
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: September 2, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2021–19405 Filed 9–8–21; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 172
[Docket No. FDA–2021–F–0926]
Monaghan Mushrooms Ireland
Unlimited Company; Filing of Food
Additive Petition
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notification of petition.
The Food and Drug
Administration (FDA or we) is
announcing that we have filed a
petition, submitted by Monaghan
Mushrooms Ireland Unlimited
Company, proposing that the food
additive regulations be amended to
provide for the safe use of vitamin D2
mushroom powder produced by
exposing dried and powdered edible
cultivars of Agaricus bisporus to
ultraviolet light.
DATES: The food additive petition was
filed on June 8, 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:
Katie Overbey, Center for Food Safety
and Applied Nutrition, Food and Drug
Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–7536.
SUPPLEMENTARY INFORMATION: Under the
Federal Food, Drug, and Cosmetic Act
(section 409(b)(5) (21 U.S.C. 348(b)(5)),
we are giving notice that we have filed
lotter on DSK11XQN23PROD with PROPOSALS1
SUMMARY:
VerDate Sep<11>2014
17:23 Sep 08, 2021
Jkt 253001
a food additive petition (FAP 1A4828),
submitted by Monaghan Mushrooms
Ireland Unlimited Company, Tullygony,
Tyholland, County Monaghan, H18
FW95, Ireland. The petition proposes to
amend the food additive regulations in
§ 172.382 (21 CFR 172.382) Vitamin D2
mushroom powder to provide for the
safe use of vitamin D2 mushroom
powder produced by exposing dried and
powdered edible cultivars of Agaricus
bisporus to ultraviolet light.
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: September 2, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for
Policy.
[FR Doc. 2021–19409 Filed 9–8–21; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF LABOR
Mine Safety and Health Administration
30 CFR Parts 56, 57 and 77
[Docket No. MSHA–2018–0016]
RIN 1219–AB91
Safety Program for Surface Mobile
Equipment
Mine Safety and Health
Administration, Labor.
ACTION: Proposed rule; request for
comments.
AGENCY:
The Mine Safety and Health
Administration (MSHA) is proposing to
require that mine operators employing
six or more miners develop and
implement a written safety program for
mobile and powered haulage equipment
(excluding belt conveyors) at surface
mines and surface areas of underground
mines. The written safety program
would include actions mine operators
would take to identify hazards and risks
to reduce accidents, injuries, and
fatalities related to surface mobile
SUMMARY:
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equipment. The proposal would offer
mine operators flexibility to devise a
safety program that is appropriate for
their specific mining conditions and
operations.
Comments must be received or
postmarked by midnight Eastern Time
on November 8, 2021.
ADDRESSES: Submit comments and
informational materials, identified by
RIN 1219–AB91 or Docket No. MSHA–
2018–0016 by one of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the online
instructions for submitting comments.
• Email: zzMSHA-comments@
dol.gov.
• Mail: MSHA, Office of Standards,
Regulations, and Variances, 201 12th
Street South, Suite 4E401, Arlington,
Virginia 22202–5452.
• Hand Delivery or Courier: 201 12th
Street South, Suite 4E401, Arlington,
Virginia, between 9:00 a.m. and 5:00
p.m. Monday through Friday, except
federal holidays. Before visiting MSHA
in person, call 202–693–9455 to make
an appointment, in keeping with the
Department of Labor’s COVID–19
policy. Special health precautions may
be required.
• Fax: 202–693–9441.
Instructions: All submissions must
include RIN 1219–AB91 or Docket No.
MSHA 2018–0016. Do not include
personal or proprietary information that
you do not wish to disclose publicly. If
a commenter marks parts of a comment
as ‘‘business confidential’’ information,
MSHA will not post those parts of the
comment. Otherwise, MSHA will post
all comments without change, including
personal information.
Docket: For access to the docket to
read comments and background
documents, go to https://
www.regulations.gov. The docket can
also be reviewed in person at MSHA,
Office of Standards, Regulations, and
Variances, 201 12th Street South,
Arlington, Virginia, between 9:00 a.m.
and 5:00 p.m. Monday through Friday,
except federal holidays. Before visiting
MSHA in person, call 202–693–9455 to
make an appointment, in keeping with
the Department of Labor’s COVID–19
policy. Special health precautions may
be required.
Email Notification: To subscribe to
receive an email notification when
MSHA publishes rulemaking documents
in the Federal Register, go to https://
public.govdelivery.com/accounts/
USDOL/subscriber/new.
Information Collection Requirements:
Comments concerning the information
collection requirements of this proposal
DATES:
E:\FR\FM\09SEP1.SGM
09SEP1
Agencies
[Federal Register Volume 86, Number 172 (Thursday, September 9, 2021)]
[Proposed Rules]
[Pages 50495-50496]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19405]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 73
[Docket No. FDA-2021-C-0925]
Fermentalg; Filing of Color Additive Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Notification of petition.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is announcing
that we have filed a petition, submitted by Fermentalg, proposing that
the color additive 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, 301-348-1740.
SUPPLEMENTARY INFORMATION: Under section 721(d)(1) the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 379e(d)(1)), we are giving notice
that we have filed a color additive petition (CAP 1C0320), submitted by
Fermentalg, 4 Rue Rivi[egrave]re, 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, non-alcoholic; (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 25.32(r) 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
[[Page 50496]]
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: September 2, 2021.
Lauren K. Roth,
Acting Principal Associate Commissioner for Policy.
[FR Doc. 2021-19405 Filed 9-8-21; 8:45 am]
BILLING CODE 4164-01-P