{"database": "openregs", "table": "dockets", "rows": [["FDA-2025-P-6262", "FDA", "Requests that FDA, under FDCA \u00a7505G(b) (OTC monograph administrative order process), amend OTC Monograph M013 to update Drug Facts labeling for all over-the-counter acetaminophen-containing products. In the alternative, Petitioner asks FDA to initiate such an order on its own", "Nonrulemaking", "2026-05-15T17:03:33Z", "0b000064b90874c3"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2025-P-6262"], "units": {}, "query_ms": 0.40803407318890095, "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"}