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withdrawn,object_id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-2007-D-0429-0033,FDA,FDA-2007-D-0429,Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals,Notice,Notice of Approval,2019-08-07T04:00:00Z,2019,8,2019-08-07T04:00:00Z,,2019-08-08T15:07:51Z,2019-16889,0,0,0900006483e0818d
FDA-2007-D-0429-0032,FDA,FDA-2007-D-0429,Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act,Notice,Announcement,2019-05-30T04:00:00Z,2019,5,2019-05-30T04:00:00Z,2019-07-02T03:59:59Z,2019-05-30T15:21:15Z,2019-11295,0,0,0900006483cd5a65
FDA-2007-D-0429-0031,FDA,FDA-2007-D-0429,Form FDA 3500A,Other,Forms,2019-02-13T05:00:00Z,2019,2,2019-02-13T05:00:00Z,,2019-02-13T17:10:33Z,,0,0,0900006483a6ea4e
FDA-2007-D-0429-0030,FDA,FDA-2007-D-0429,Guidance for Industry Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act:  Questions andAnswers,Other,Guidance,2019-02-13T05:00:00Z,2019,2,2019-02-13T05:00:00Z,,2024-11-12T22:54:24Z,,1,0,0900006483a6e08b
FDA-2007-D-0429-0029,FDA,FDA-2007-D-0429,Agency Information Collection Activities; Proposed Collection; Comment Request; Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary  Supplement and Nonprescription Drug Consumer Protection Act,Notice,60 Day Proposed Information Collection,2019-02-11T05:00:00Z,2019,2,2019-02-11T05:00:00Z,2019-04-13T03:59:59Z,2019-02-11T13:02:25Z,2019-01793,0,0,0900006483a5e875
FDA-2007-D-0429-0028,FDA,FDA-2007-D-0429,"Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approvals",Notice,Notice of Approval,2016-07-11T04:00:00Z,2016,7,2016-07-11T04:00:00Z,,2016-07-11T13:30:49Z,2016-16349,0,0,090000648209c0b1
FDA-2007-D-0429-0027,FDA,FDA-2007-D-0429,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Guidance for
Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved
Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act",Notice,30 Day Proposed Information Collection,2016-02-19T05:00:00Z,2016,2,2016-02-19T05:00:00Z,2016-03-22T03:59:59Z,2016-02-19T17:57:33Z,2016-03457,0,0,0900006481e784fc
FDA-2007-D-0429-0025,FDA,FDA-2007-D-0429,"Agency Information Collection Activities; Proposed Collection;
Comment Request; Guidance for Industry on Questions and Answers
Regarding the Labeling of Nonprescription Human Drug Products
Marketed Without an Approved Application as Required by the Dietary
Supplement and Nonprescription Drug Consumer Protection Act",Notice,60 Day Proposed Information Collection,2015-07-17T04:00:00Z,2015,7,2015-07-17T04:00:00Z,2015-09-16T03:59:59Z,2015-08-17T01:30:28Z,2015-17558,0,0,0900006481b8ea02
FDA-2007-D-0429-0024,FDA,FDA-2007-D-0429,"Agency Information Collection Activities; Proposals, Submissions, and Approvals: Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application, etc.",Notice,N-Notice,2011-02-08T05:00:00Z,2011,2,2011-02-08T05:00:00Z,,2015-07-07T11:47:54Z,2011-02662,0,0,0900006480be0eeb
FDA-2007-D-0429-0022,FDA,FDA-2007-D-0429,Guidance for Industry on Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers; Availability,Notice,Notice of Availability,2009-09-01T04:00:00Z,2009,9,2009-09-01T04:00:00Z,,2015-07-07T12:00:25Z,E9-21093,0,0,0900006480a1a533
FDA-2007-D-0429-0023,FDA,FDA-2007-D-0429,Guidance for Industry on Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers - Guidance,Other,Guidance,2009-09-01T04:00:00Z,2009,9,2009-09-01T04:00:00Z,,2015-07-07T12:01:46Z,,0,0,0900006480a1a6d4
FDA-2007-D-0429-0021,FDA,FDA-2007-D-0429,"Agency Information Collection Activities; Proposals, Submissions, and Approvals",Notice,N-Notice,2009-02-24T05:00:00Z,2009,2,2009-02-24T05:00:00Z,2009-03-27T03:59:59Z,2015-07-07T11:54:46Z,E9-03917,0,0,09000064808d6ce8
FDA-2007-D-0429-0016,FDA,FDA-2007-D-0429,Congress of the United States - Letter,Other,LET-Letter,2009-01-14T05:00:00Z,2009,1,2009-01-14T05:00:00Z,,2009-01-14T13:52:56Z,,0,0,090000648081d612
FDA-2007-D-0429-0018,FDA,FDA-2007-D-0429,Memorandum of Meeting,Other,MM-Memorandum of Meeting,2009-01-14T05:00:00Z,2009,1,2009-01-14T05:00:00Z,,2009-01-14T13:52:59Z,,0,0,090000648081d645
FDA-2007-D-0429-0017,FDA,FDA-2007-D-0429,United States Senate - Letter,Other,LET-Letter,2009-01-14T05:00:00Z,2009,1,2009-01-14T05:00:00Z,,2009-01-14T13:52:57Z,,0,0,090000648081d62e
FDA-2007-D-0429-0014,FDA,FDA-2007-D-0429,Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Revision 1; Availability,Notice,Notice of Availability,2008-12-11T05:00:00Z,2008,12,2008-12-11T05:00:00Z,,2019-08-20T11:52:24Z,E8-29301,0,0,09000064807d7084
FDA-2007-D-0429-0015,FDA,FDA-2007-D-0429,Guidance for Industry - Question and Answers regarding the labeling of nonprescription human drug products marketed without an approved application as reqired by the dietary supplement and nonprescription drug consumer protection act: revision 1,Supporting & Related Material,Guidance,2008-12-11T05:00:00Z,2008,12,,,2015-07-07T11:58:17Z,,0,0,09000064807d71ee
FDA-2007-D-0429-0012,FDA,FDA-2007-D-0429,"The Honorable Orrin G. Hatch to the Assistant Commissioner for Policy, FDA - Letter",Other,LET-Letter,2008-06-17T04:00:00Z,2008,6,2008-06-17T04:00:00Z,,2008-06-17T14:38:14Z,,0,0,090000648062ac2d
FDA-2007-D-0429-0003,FDA,FDA-2007-D-0429,Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability,Notice,Notice of Availability,2008-06-16T04:00:00Z,2008,6,2008-06-16T04:00:00Z,,2015-07-07T11:49:55Z,07–6267,0,0,09000064806294d9
FDA-2007-D-0429-0004,FDA,FDA-2007-D-0429,Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Draft Guidance Document,Other,Guidance,2008-06-16T04:00:00Z,2008,6,2008-01-02T19:57:32Z,,2019-08-20T11:51:45Z,,0,0,0900006480629527
FDA-2007-D-0429-0001,FDA,FDA-2007-D-0429,NO DOCUMENT POSTED - See FDA-2007-D-0429-0003,Supporting & Related Material,BKG- Background Material (internal references),2008-01-02T05:00:00Z,2008,1,,,2008-06-17T00:41:15Z,,0,0,090000648042dc0a
FDA-2007-D-0429-0002,FDA,FDA-2007-D-0429,NO DOCUMENT POSTED - See FDA-2007-D-0429-0004,Supporting & Related Material,GDL-Guidance,2008-01-02T05:00:00Z,2008,1,,,2008-06-17T00:42:14Z,,0,0,090000648042dc0d