{"description":"Documents matching '\"Modernization of Cosmetics Regulation Act\"'","count":12,"total_pages":1,"results":[{"title":"Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products; Withdrawal","type":"Proposed Rule","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the withdrawal of the proposed rule entitled \"Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products,\" which published in the Federal Register of December 27, 2024. FDA is taking this action in response to comments received during the comment period for the proposed rule that warrant further consideration and assessment prior to issuing final regulations to establish and require standardized testing methods for detecting and identifying asbestos in talc-containing cosmetic products pursuant to the Modernization of Cosmetics Regulation Act of 2022.","document_number":"2025-21407","html_url":"https://www.federalregister.gov/documents/2025/11/28/2025-21407/testing-methods-for-detecting-and-identifying-asbestos-in-talc-containing-cosmetic-products","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-11-28/pdf/2025-21407.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-21407.pdf?1764078345","publication_date":"2025-11-28","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"period for the proposed rule that warrant further consideration and assessment prior to issuing final regulations to establish and require standardized testing methods for detecting and identifying asbestos in talc-containing cosmetic products pursuant to the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022.\n \n \n \n DATES: \n The proposed rule published December 27, 2024 (89 FR 105490) is withdrawn as of November 28, 2025. \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n Elizabeth Anderson, Senior Policy Analyst, Food and Drug Administration, 240-402-4565, "},{"title":"Registration and Listing of Cosmetic Product Facilities and Products; Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a final guidance for industry entitled \"Registration and Listing of Cosmetic Product Facilities and Products.\" The guidance will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). This guidance includes three new draft frequently asked questions and answers about cosmetic product facility registrations and product listing submissions, in Appendix B, for comment purposes only. Aside from the three new draft frequently asked questions and answers, this guidance finalizes the draft Appendix B published in an otherwise final guidance on December 19, 2023. This guidance also includes minor changes to the final guidance for clarity.","document_number":"2024-29237","html_url":"https://www.federalregister.gov/documents/2024/12/12/2024-29237/registration-and-listing-of-cosmetic-product-facilities-and-products-guidance-for-industry","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-12-12/pdf/2024-29237.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-29237.pdf?1733924742","publication_date":"2024-12-12","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"availability of a final guidance for industry entitled “Registration and Listing of Cosmetic Product Facilities and Products.” The guidance will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). This guidance includes three new draft frequently asked questions and answers about cosmetic product facility registrations and product listing submissions, in Appendix B, for comment purposes only. Aside from the three new draft frequently"},{"title":"Questions and Answers Regarding Mandatory Cosmetics Recalls: Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance document entitled \"Questions and Answers Regarding Mandatory Cosmetics Recalls: Guidance for Industry.\" The draft guidance document, when finalized, will provide answers to common questions that might arise about FDA's mandatory recall authority for cosmetics. It is intended to inform regulated industry about the Agency's current thinking on implementation of certain aspects, including the criteria, process, and expectations, for mandatory recalls of cosmetic products.","document_number":"2025-23249","html_url":"https://www.federalregister.gov/documents/2025/12/18/2025-23249/questions-and-answers-regarding-mandatory-cosmetics-recalls-draft-guidance-for-industry-availability","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-12-18/pdf/2025-23249.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-23249.pdf?1765979123","publication_date":"2025-12-18","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"document, when finalized, is to provide guidance to industry on the implementation of the mandatory cosmetics recall provisions of section 611 of the Federal Food, Drug, and Cosmetic Act (the FD&amp;C Act or the Act), which was added by section 3502 of the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). The guidance is in the form of Questions and Answers and provides answers to common questions that might arise about these mandatory recall provisions and FDA's current thinking regarding their implementation. \n This draft guidance is being"},{"title":"FDA Records Access Authority for Cosmetics; Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft document entitled \"FDA Records Access Authority for Cosmetics: Guidance for Industry.\" The draft guidance document provides answers to frequently asked questions about certain authorities for FDA to access records related to cosmetic products. It is intended to inform regulated industry about the Agency's current thinking regarding the criteria, process, and expectations for FDA's access to these records.","document_number":"2026-01159","html_url":"https://www.federalregister.gov/documents/2026/01/22/2026-01159/fda-records-access-authority-for-cosmetics-draft-guidance-for-industry-availability","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-22/pdf/2026-01159.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01159.pdf?1769003114","publication_date":"2026-01-22","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"is not binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the applicable statutes and regulations. \n On December 29, 2022, the Consolidated Appropriations Act, 2023 (Pub. L. 117-328), which included the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA), was signed into law. Among other provisions, MoCRA added sections 605 (21 U.S.C. 364a) and 610 (21 U.S.C. 364f) to, and amended section 704(a)(1) (21 U.S.C. 374(a)(1)) of, the Federal Food, Drug, and Cosmetic Act (FD&amp;C Act), establishing"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; Requirements for Cosmetic Products","type":"Notice","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection activity requirements for cosmetic products.","document_number":"2026-14434","html_url":"https://www.federalregister.gov/documents/2026/07/17/2026-14434/agency-information-collection-activities-proposed-collection-comment-request-requirements-for","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-07-17/pdf/2026-14434.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-14434.pdf?1784205916","publication_date":"2026-07-17","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Requirements for Cosmetic Products \n OMB Control Number 0910-0599—Revision \n This information collection supports implementation of statutory and regulatory requirements that govern cosmetic products, including requirements most recently established under the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). MoCRA amended the Federal Food, Drug, and Cosmetic Act by adding, in pertinent part, sections 604, 605, 607, 608, and 609 (21 U.S.C. 364b, 364c, 364e, and 364g), which establish or amend definitions and requirements related to adverse events"},{"title":"Registration and Listing of Cosmetic Product Facilities and Products; Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or we) is announcing the availability of a final guidance for industry entitled \"Registration and Listing of Cosmetic Product Facilities and Products.\" The guidance will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). This guidance also includes a new draft section, Appendix B, for comment purposes only, that describes frequently asked questions and answers about cosmetic product facility registrations and product listing submissions. Aside from that section, this guidance finalizes the draft guidance that was published on August 8, 2023.","document_number":"2023-27649","html_url":"https://www.federalregister.gov/documents/2023/12/19/2023-27649/registration-and-listing-of-cosmetic-product-facilities-and-products-guidance-for-industry","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-12-19/pdf/2023-27649.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-27649.pdf?1702907116","publication_date":"2023-12-19","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"availability of a final guidance for industry entitled “Registration and Listing of Cosmetic Product Facilities and Products.” The guidance will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). This guidance also includes a new draft section, Appendix B, for comment purposes only, that describes frequently asked questions and answers about cosmetic product facility registrations and product listing submissions. Aside from that section"},{"title":"Registration and Listing of Cosmetic Product Facilities and Products; Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a draft guidance for industry entitled \"Registration and Listing of Cosmetic Product Facilities and Products.\" This draft guidance, when finalized, will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). This draft guidance is not final nor is it in effect at this time.","document_number":"2023-16771","html_url":"https://www.federalregister.gov/documents/2023/08/08/2023-16771/registration-and-listing-of-cosmetic-product-facilities-and-products-draft-guidance-for-industry","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-08-08/pdf/2023-16771.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-16771.pdf?1691412320","publication_date":"2023-08-08","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"guidance for industry entitled “Registration and Listing of Cosmetic Product Facilities and Products.” This draft guidance, when finalized, will assist persons submitting cosmetic product facility registrations and product listing submissions to FDA under the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). This draft guidance is not final nor is it in effect at this time. \n \n \n DATES: \n Submit either electronic or written comments on the draft guidance by September 7, 2023 to ensure that the Agency considers your comment on this draft guidance"},{"title":"Pilot Program for Cosmetic Product Facility Registration and Listing Electronic Submissions User Acceptance Testing","type":"Notice","abstract":"The Office of Cosmetics and Colors (OCAC) and the Office of the Chief Scientist (OCS) in the Food and Drug Administration (FDA, Agency, or we) are soliciting applications from members of the cosmetic product industry interested in participating in a voluntary pilot program to conduct user acceptance testing to help OCAC and OCS evaluate a potential new electronic submissions portal for cosmetic product facility registration and listing. This electronic submission portal is being implemented pursuant to the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). OCAC and OCS plan to accept up to nine participants for the pilot program. The pilot program is intended to provide OCAC and OCS input to inform evaluation of this new electronic submission portal.","document_number":"2023-16772","html_url":"https://www.federalregister.gov/documents/2023/08/08/2023-16772/pilot-program-for-cosmetic-product-facility-registration-and-listing-electronic-submissions-user","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-08-08/pdf/2023-16772.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-16772.pdf?1691412321","publication_date":"2023-08-08","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"voluntary pilot program to conduct user acceptance testing to help OCAC and OCS evaluate a potential new electronic submissions portal for cosmetic product facility registration and listing. This electronic submission portal is being implemented pursuant to the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). OCAC and OCS plan to accept up to nine participants for the pilot program. The pilot program is intended to provide OCAC and OCS input to inform evaluation of this new electronic submission portal. \n \n \n DATES: \n Interested parties should"},{"title":"Compliance Policy for Cosmetic Product Facility Registration and Cosmetic Product Listing; Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or we) is announcing the availability of a final guidance for industry and the public on the requirements related to cosmetic product facility registration and cosmetic product listing under the Federal Food, Drug, and Cosmetic Act (FD&C Act) entitled \"Compliance Policy for Cosmetic Product Facility Registration and Cosmetic Product Listing.\" This guidance announces FDA's intention to delay enforcement of the requirements related to cosmetic product facility registration and cosmetic product listing for an additional 6 months after the initial December 29, 2023, deadline.","document_number":"2023-24731","html_url":"https://www.federalregister.gov/documents/2023/11/09/2023-24731/compliance-policy-for-cosmetic-product-facility-registration-and-cosmetic-product-listing-guidance","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-11-09/pdf/2023-24731.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-24731.pdf?1699451168","publication_date":"2023-11-09","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"document is immediately in effect, it remains subject to comment in accordance with FDA's GGP regulation ((§ 10.115(g)(5)).\n \n On December 29, 2022, the President signed the Consolidated Appropriations Act, 2023 (Pub. L. 117-328) into law, which included the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). Among other provisions, MoCRA added section 607 to the FD&amp;C Act, establishing requirements for cosmetic product facility registration and product listing. Section 607 of the FD&amp;C Act generally imposes an initial registration and listing"},{"title":"Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products","type":"Proposed Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is proposing to require testing of talc-containing cosmetic products using standardized testing methods for detecting and identifying asbestos that may be present as a contaminant in talc. We are also proposing corresponding adulteration provisions. Asbestos is a potential contaminant in talc, which is used in certain cosmetic products, and is a known human carcinogen. This proposed rule, if finalized, will help protect users of talc-containing cosmetic products from harmful exposure to asbestos given the potential for contamination of these products.","document_number":"2024-30544","html_url":"https://www.federalregister.gov/documents/2024/12/27/2024-30544/testing-methods-for-detecting-and-identifying-asbestos-in-talc-containing-cosmetic-products","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-12-27/pdf/2024-30544.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-30544.pdf?1735220714","publication_date":"2024-12-27","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Impact \n IX. Paperwork Reduction Act of 1995 \n X. Federalism \n XI. Consultation and Coordination With Indian Tribal Governments \n XII. References \n \n I. Executive Summary \n A. Purpose of the Proposed Rule \n We are issuing this proposed rule pursuant to the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA), which requires the promulgation of proposed and final regulations to establish and require standardized testing methods for detecting and identifying asbestos in talc-containing cosmetic products. This proposed rule, if finalized, will help"},{"title":"Statement of Organization, Functions, and Delegations of Authority","type":"Notice","abstract":"The Food and Drug Administration (FDA), Office of the Commissioner, Headquarters organizations, and Centers have modified their organizational structure","document_number":"2024-11893","html_url":"https://www.federalregister.gov/documents/2024/06/03/2024-11893/statement-of-organization-functions-and-delegations-of-authority","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-06-03/pdf/2024-11893.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-11893.pdf?1717082112","publication_date":"2024-06-03","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"health mission; provide employees with clearer priorities and more career opportunities; and comply with recent legislation such as the Food and Drug Omnibus Reform Act of 2022 (FDORA) mandating the establishment of the Office of Critical Foods, and the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA) to ensure the safety of cosmetics products. \n The reorganization establishes the HFP by realigning the functions of the Center for Food Safety and Applied Nutrition (CFSAN), Office of Food Policy and Response, as well as key functions from"},{"title":"Good Manufacturing Practices for Cosmetic Products Listening Session; Public Meeting; Request for Comments","type":"Notice","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing a virtual listening session entitled ``Good Manufacturing Practices for Cosmetic Products Listening Session.'' The purpose of the listening session is to consult cosmetics manufacturers, including smaller businesses, consumer organizations, and other experts, to inform Agency efforts to develop regulations to establish good manufacturing practices for facilities that manufacture or process cosmetic products distributed in the United States.","document_number":"2023-08942","html_url":"https://www.federalregister.gov/documents/2023/04/27/2023-08942/good-manufacturing-practices-for-cosmetic-products-listening-session-public-meeting-request-for","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-04-27/pdf/2023-08942.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-08942.pdf?1682513137","publication_date":"2023-04-27","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"is not a toll-free number), email: \n MoCRAGMPMeeting@fda.hhs.gov. \n \n \n \n \n SUPPLEMENTARY INFORMATION: \n \n I. Background \n On December 29, 2022, the President signed the Consolidated Appropriations Act, 2023 (Pub. L. 117–328) into law, which included the <span class=\"match\">Modernization of Cosmetics Regulation Act</span> of 2022 (MoCRA). Among other provisions, MoCRA added section 606 to the Federal Food, Drug, and Cosmetic Act (FD&amp;C Act), requiring FDA to establish by regulation good manufacturing practices (GMPs) for facilities that manufacture or process cosmetic products"}]}