{"database": "lobbying", "table": "lobbying_activities", "rows": [[1195514, "536c456c-d184-44a4-9b85-99d386b35335", "Q4", "CONSUMER HEALTHCARE PRODUCTS ASSOCIATION", 29403, "CONSUMER HEALTHCARE PRODUCTS ASSOCIATION", 2011, "fourth_quarter", "PHA", "Over-the-Counter (OTC) medicines; Manufacturing and importation of OTC drugs; mandatory recall authority of the FDA H.R. 1483 - Drug Safety Enhancement Act of 2011.  Amends the federal Food, Drug, and Cosmetic Act (FDCA) to expand drug establishment registration requirements to include foreign drug establishments and other purposes; all sections.\n\nS. 1584 - Drug Safety and Accountability Act of 2011.  Amends the federal Food, Drug, and Cosmetic Act (FDCA) to expand registration requirements for drug manufacturers, wholesalers, distributors, and retailers; grants FDA mandatory recall authority; requires adequate documentation of the pharmaceutical supply chain; all sections.", "Food & Drug Administration (FDA),HOUSE OF REPRESENTATIVES,SENATE", null, 180000, 0, 0, "2012-01-19T13:12:34-05:00"]], "columns": ["id", "filing_uuid", "filing_type", "registrant_name", "registrant_id", "client_name", "filing_year", "filing_period", "issue_code", "specific_issues", "government_entities", "income_amount", "expense_amount", "is_no_activity", "is_termination", "received_date"], "primary_keys": ["id"], "primary_key_values": ["1195514"], "units": {}, "query_ms": 4.537271102890372, "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"}