id,agency_id,docket_id,title,document_type,subtype,posted_date,posted_year,posted_month,comment_start_date,comment_end_date,last_modified,fr_doc_num,open_for_comment,withdrawn,object_id
FDA-2013-N-0823-0002,FDA,FDA-2013-N-0823,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Over-the-Counter Drugs; Labeling Requirements,Notice,30 Day Proposed Information Collection,2013-12-05T05:00:00Z,2013,12,2013-12-05T05:00:00Z,2014-01-07T04:59:59Z,2013-12-08T15:37:58Z,2013-29079,0,0,09000064814a9e18
FDA-2013-N-0823-0001,FDA,FDA-2013-N-0823,Agency Information Collection Activities: Proposed Collection; Comment Request; Format and Content Requirements for Over-the-Counter Drug Product Labeling,Notice,60 Day Proposed Information Collection,2013-07-23T04:00:00Z,2013,7,2013-07-23T04:00:00Z,2013-09-24T03:59:59Z,2013-12-08T15:39:05Z,2013-17548,0,0,09000064813761d3