documents: FDA-2007-D-0429-0014

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2007-D-0429-0014 FDA FDA-2007-D-0429 Draft Guidance for Industry on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the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

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