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withdrawn,object_id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-0823-0005,FDA,FDA-2013-N-0823,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Format and
Content Requirements for Over-the-Counter Drug Product Labeling",Notice,30 Day Proposed Information Collection,2016-10-26T04:00:00Z,2016,10,2016-10-26T04:00:00Z,2016-11-26T04:59:59Z,2016-11-20T14:00:34Z,2016-25854,0,0,090000648234d49e
FDA-2013-N-0823-0004,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,2016-04-01T04:00:00Z,2016,4,2016-04-01T04:00:00Z,2016-06-01T03:59:59Z,2016-10-18T18:13:40Z,2016-07369,0,0,0900006481f09282