{"abstract":"The Food and Drug Administration (FDA) is announcing a public hearing to obtain information and comments from stakeholders about the current use of human drug and biological products labeled as homeopathic, as well as the Agency's regulatory framework for such products. These products include prescription drugs and biological products labeled as homeopathic and over-the-counter (OTC) drugs labeled as homeopathic. FDA is seeking participants for the public hearing and written comments from all interested parties, including, but not limited to, consumers, patients, caregivers, health care professionals, patient groups, and industry. FDA is seeking input on a number of specific questions, but is interested in any other pertinent information participants would like to share.","action":"Notice of public hearing; request for comments.","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/2015/03/27/2015-07018.html","cfr_references":[{"chapter":null,"citation_url":null,"part":15,"title":21}],"citation":"80 FR 16327","comment_url":null,"comments_close_on":"2015-06-22","correction_of":null,"corrections":[],"dates":"The public hearing will be held on April 20 and 21, 2015, from 9 a.m. to 4 p.m. The meeting may be extended or may end early depending on the level of public participation. Register to attend or provide oral testimony at the hearing by April 13, 2015. See Registration and Request to Provide Oral Testimony for information on how to register or make an oral presentation at the hearing. Written or electronic comments will be accepted until June 22, 2015.","disposition_notes":null,"docket_ids":["Docket No. FDA-2015-N-0540"],"dockets":[{"supporting_documents":[],"agency_name":null,"documents":[{"comment_count":7820,"comment_start_date":"2015-03-27","updated_at":"2023-02-28T20:14:43.142-05:00","comment_url":"https://www.regulations.gov/commenton/FDA-2015-N-0540-0001","allow_late_comments":null,"id":"FDA-2015-N-0540-0001","comment_end_date":"2015-06-23","regulations_dot_gov_open_for_comment":false}],"supporting_documents_count":0,"id":"FDA-2015-N-0540","title":"Homeopathic Product Regulation: Evaluating FDA’s Regulatory Framework After a Quarter-Century"}],"document_number":"2015-07018","effective_on":null,"end_page":16329,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2015/03/27/2015-07018.xml","html_url":"https://www.federalregister.gov/documents/2015/03/27/2015-07018/homeopathic-product-regulation-evaluating-the-food-and-drug-administrations-regulatory-framework","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2015-07018?publication_date=2015-03-27","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2015-03-27/2015-07018/mods.xml","not_received_for_publication":null,"page_length":3,"page_views":{"count":9831,"last_updated":"2026-10-22 14:15:05 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2015-03-27/pdf/2015-07018.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2015-07018.pdf?1427373990","publication_date":"2015-03-27","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2015/03/27/2015-07018.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[],"comments_count":7820,"agency_id":"FDA","comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2015-N-0540","supporting_documents_count":0,"docket_id":"FDA-2015-N-0540","document_id":"FDA-2015-N-0540-0001","regulation_id_number":null,"title":"Homeopathic Product Regulation: Evaluating FDA’s Regulatory Framework After a Quarter-Century","checked_regulationsdotgov_at":"2023-03-01T01:14:42Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":16327,"subtype":null,"title":"Homeopathic Product Regulation: Evaluating the Food and Drug Administration's Regulatory Framework After a Quarter-Century; Public Hearing","toc_doc":"Evaluating Regulatory Framework After a Quarter-Century; Public Hearing","toc_subject":"Homeopathic Products:","topics":[],"type":"Proposed Rule","volume":80}