{"abstract":"The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.","action":"Notice.","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"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2016/01/21/2016-01103.html","cfr_references":[],"citation":"81 FR 3438","comment_url":null,"comments_close_on":"2016-02-22","correction_of":null,"corrections":[],"dates":"Fax written comments on the collection of information by February 22, 2016.","disposition_notes":null,"docket_ids":["Docket No. FDA-2007-D-0372"],"dockets":[{"supporting_documents":[{"title":"Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act - Suporting Statement","document_id":"FDA-2007-D-0372-0011"},{"title":"References","document_id":"FDA-2007-D-0372-0003"},{"title":"Guidance","document_id":"FDA-2007-D-0372-0002"}],"agency_name":null,"documents":[{"comment_count":0,"comment_start_date":"2016-01-21","updated_at":"2023-02-28T16:28:38.904-05:00","comment_url":"https://www.regulations.gov/commenton/FDA-2007-D-0372-0015","allow_late_comments":null,"id":"FDA-2007-D-0372-0015","comment_end_date":"2016-02-23","regulations_dot_gov_open_for_comment":false}],"supporting_documents_count":3,"id":"FDA-2007-D-0372","title":"Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act"}],"document_number":"2016-01103","effective_on":null,"end_page":3439,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2016/01/21/2016-01103.xml","html_url":"https://www.federalregister.gov/documents/2016/01/21/2016-01103/agency-information-collection-activities-submission-for-office-of-management-and-budget-review","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2016-01103?publication_date=2016-01-21","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2016-01-21/2016-01103/mods.xml","not_received_for_publication":null,"page_length":2,"page_views":{"count":151,"last_updated":"2026-08-26 10:15:07 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2016-01-21/pdf/2016-01103.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2016-01103.pdf?1453297599","publication_date":"2016-01-21","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2016/01/21/2016-01103.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[{"title":"Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act - Suporting Statement","document_id":"FDA-2007-D-0372-0011"},{"title":"References","document_id":"FDA-2007-D-0372-0003"},{"title":"Guidance","document_id":"FDA-2007-D-0372-0002"}],"comments_count":0,"agency_id":"FDA","comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2007-D-0372","supporting_documents_count":3,"docket_id":"FDA-2007-D-0372","document_id":"FDA-2007-D-0372-0015","regulation_id_number":null,"title":"Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act","checked_regulationsdotgov_at":"2023-02-28T21:28:38Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":3438,"subtype":null,"title":"Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act","toc_doc":"Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act","toc_subject":"Agency Information Collection Activities; Proposals, Submissions, and Approvals:","topics":[],"type":"Notice","volume":81}