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withdrawn,object_id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-1978-N-0018-0741,FDA,FDA-1978-N-0018,"Bare Escentuals Beauty, Inc. - Citizen Petition",Other,Citizen Petition,2011-11-04T04:00:00Z,2011,11,2011-11-04T04:00:00Z,,2024-11-07T22:40:16Z,,1,0,0900006480f54fcd
FDA-1978-N-0018-0742,FDA,FDA-1978-N-0018,Acknowledgement Letter to Bare Escentuals Beauty Inc.,Other,Acknowledgement Letter/Receipt,2011-11-04T04:00:00Z,2011,11,2011-11-04T04:00:00Z,,2011-11-04T23:20:06Z,,0,0,0900006480f550f6
FDA-1978-N-0018-0707,FDA,FDA-1978-N-0018,"Energizer Personal Care, LLC (EPC) - Request for Extension",Other,Request for Extension,2011-09-16T04:00:00Z,2011,9,2011-09-16T04:00:00Z,,2011-09-16T14:40:39Z,,0,0,0900006480ee2067
FDA-1978-N-0018-0706,FDA,FDA-1978-N-0018,Sunscreen Drug Products for Over-the-Counter Human Use: Request for Data and Information Regarding Dosage Forms; Extension of Comment Period,Proposed Rule,Notice of Extension,2011-09-14T04:00:00Z,2011,9,2011-09-14T04:00:00Z,2011-10-18T03:59:59Z,2012-03-24T19:28:47Z,2011-23479,0,0,0900006480f19657
FDA-1978-N-0018-0705,FDA,FDA-1978-N-0018,Personal Care Products Council - Request for Extension,Other,Request for Extension,2011-09-12T04:00:00Z,2011,9,2011-09-12T04:00:00Z,,2011-09-12T22:44:37Z,,0,0,0900006480edf5d9
FDA-1978-N-0018-0701,FDA,FDA-1978-N-0018,Merck Consumer Care - Request for Extension Comment Due Date,Other,Request for Extension,2011-07-08T04:00:00Z,2011,7,2011-07-08T04:00:00Z,,2011-08-12T15:40:51Z,,0,0,0900006480ebd0b1
FDA-1978-N-0018-0700,FDA,FDA-1978-N-0018,Labeling and Effectiveness Testing: Sunscreen Drug Products for Over-the-Counter Human Use - Notice of Correction,Notice,Correction,2011-07-05T04:00:00Z,2011,7,2011-07-05T04:00:00Z,,2012-04-25T12:46:12Z,C1-2011-14766,0,0,0900006480eb965e
FDA-1978-N-0018-0697,FDA,FDA-1978-N-0018,Sunscreen Drug Products for Over-the-Counter Human Use; Request for Data and Information Regarding Dosage Forms,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2011-06-17T04:00:00Z,2011,6,2011-06-17T04:00:00Z,2011-09-16T03:59:59Z,2011-08-12T15:28:51Z,2011-14768,0,0,0900006480e51fc3
FDA-1978-N-0018-0698,FDA,FDA-1978-N-0018,Labeling and Effectiveness Testing: Sunscreen Drug Products for Over-the-Counter Human Use,Rule,Final Rule,2011-06-17T04:00:00Z,2011,6,2011-06-17T04:00:00Z,,2017-12-07T17:18:11Z,2011-14766,0,0,0900006480e52002
FDA-1978-N-0018-0699,FDA,FDA-1978-N-0018,Revised Effectiveness Determination; Sunscreen Drug Products for Over-the-Counter Human Use,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2011-06-17T04:00:00Z,2011,6,2011-06-17T04:00:00Z,2011-09-16T03:59:59Z,2012-02-08T21:51:20Z,2011-14769,0,0,0900006480e52098
FDA-1978-N-0018-0696,FDA,FDA-1978-N-0018,"Johnson & Johnson Consumer Companies, Inc. (JJCCI) and Neutrogena Corporation, Johnson & Johnson Consumer & Personal Products Worldwide (CPPW) - Letter",Other,LET-Letter,2011-02-08T05:00:00Z,2011,2,2011-02-08T05:00:00Z,,2011-06-11T16:25:40Z,,0,0,0900006480be2d06
FDA-1978-N-0018-0695,FDA,FDA-1978-N-0018,"Johnson & Johnson Consumer Companies, Inc. - Letter",Other,LET-Letter,2011-02-08T05:00:00Z,2011,2,2011-02-08T05:00:00Z,,2013-08-11T03:12:57Z,,0,0,0900006480bd827e