{"database": "openregs", "table": "documents", "rows": [["FDA-2017-D-6580-4829", "FDA", "FDA-2017-D-6580", "Drug Products Labeled as Homeopathic Guidance for FDA Staff and Industry; Draft Guidance", "Other", "Guidance", "2019-10-25T04:00:00Z", 2019, 10, "2019-10-25T04:00:00Z", "2020-05-24T03:59:59Z", "2022-12-07T15:50:48Z", null, 0, 0, "09000064840f9370"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2017-D-6580-4829"], "units": {}, "query_ms": 106.27181699965149, "source": "Federal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"}