{"database": "openregs", "table": "documents", "rows": [["FDA-2007-D-0209-0024", "FDA", "FDA-2007-D-0209", "Guidance for Industry: Questions and Answers Regarding the Labeling of Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act; Availability", "Notice", "NAD-Notice of Availability of Data", "2009-09-01T04:00:00Z", 2009, 9, "2009-09-01T04:00:00Z", null, "2009-09-01T17:06:12Z", "E9-21094", 0, 0, "0900006480a1a478"]], "columns": ["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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2007-D-0209-0024"], "units": {}, "query_ms": 105.7801351416856, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}