Monaghan Mushrooms Ireland Unlimited Company; Filing of Food Additive Petition, 50496 [2021-19409]
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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:
PO 00000
Frm 00013
Fmt 4702
Sfmt 4702
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]
[Page 50496]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19409]
-----------------------------------------------------------------------
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.
-----------------------------------------------------------------------
SUMMARY: 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 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 Sec. 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