documents: FDA-2012-D-1086-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2012-D-1086-0002 FDA FDA-2012-D-1086 Guidance for Industry; Labeling and Effectiveness Testing; Sunscreen Drug Products for Over-the-Counter Human Use; Small Entity Compliance Guide Other Guidance 2012-12-06T05:00:00Z 2012 12 2012-12-06T05:00:00Z   2024-11-12T05:10:44Z   1 0 0900006481181139

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