documents: FDA-2007-D-0429-0023

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-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

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