Monaghan Mushrooms Ireland Unlimited Company; Filing of Food Additive Petition, 50496 [2021-19409]

Download as PDF 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]


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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
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