{"abstract":"The Food and Drug Administration (FDA) is issuing a final rule establishing a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products. This final rule is intended to assist consumers in reading and understanding OTC drug product labeling so that consumers may use these products safely and effectively. This final rule will require all OTC drug products to carry the new, easy-to-read format and the revised content requirements within prescribed implementation periods.","action":"Final rule.","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/1999/03/17/99-6296.html","cfr_references":[{"chapter":null,"citation_url":null,"part":null,"title":21},{"chapter":null,"citation_url":null,"part":"201","title":21},{"chapter":null,"citation_url":null,"part":"330","title":21},{"chapter":null,"citation_url":null,"part":"331","title":21},{"chapter":null,"citation_url":null,"part":"341","title":21},{"chapter":null,"citation_url":null,"part":"346","title":21},{"chapter":null,"citation_url":null,"part":"355","title":21},{"chapter":null,"citation_url":null,"part":"358","title":21},{"chapter":null,"citation_url":null,"part":"369","title":21},{"chapter":null,"citation_url":null,"part":"701","title":21}],"citation":"64 FR 13254","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":"April 16, 1999.","disposition_notes":null,"docket_ids":["Docket Nos. 98N-0337, 96N-0420, 95N-0259, and 90P-0201"],"dockets":[],"document_number":"99-6296","effective_on":"1999-04-16","end_page":13303,"executive_order_notes":null,"executive_order_number":null,"full_text_xml_url":null,"html_url":"https://www.federalregister.gov/documents/1999/03/17/99-6296/over-the-counter-human-drugs-labeling-requirements","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/99-6296?publication_date=1999-03-17","mods_url":"https://www.govinfo.gov/metadata/granule/FR-1999-03-17/99-6296/mods.xml","not_received_for_publication":null,"page_length":50,"page_views":{"count":1681,"last_updated":"2026-07-27 12:15:04 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-1999-03-17/pdf/99-6296.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":null,"publication_date":"1999-03-17","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/1999/03/17/99-6296.txt","regulation_id_number_info":{"0910-AA79":{"issue":"199904","html_url":"https://www.federalregister.gov/regulations/0910-AA79/over-the-counter-human-drugs-labeling-requirements","title":"Over-the-Counter Human Drugs; Labeling Requirements","xml_url":"http://www.reginfo.gov/public/do/eAgendaViewRule?pubId=199904&RIN=0910-AA79&operation=OPERATION_EXPORT_XML","priority_category":"Other Significant"}},"regulation_id_numbers":["0910-AA79"],"regulations_dot_gov_info":{"checked_regulationsdotgov_at":"2011-09-21T01:56:58Z"},"regulations_dot_gov_url":null,"significant":true,"signing_date":null,"start_page":13254,"subtype":null,"title":"Over-The-Counter Human Drugs; Labeling Requirements","toc_doc":null,"toc_subject":null,"topics":[],"type":"Rule","volume":64}