Package 84573-517-03

{"route": ["TOPICAL"], "spl_id": "2019e91f-7c9a-32bb-e063-6294a90ad6ba", "openfda": {"upc": ["0810042760325", "0810042760684", "0810042760417", "0810042760318", "0810042761001", "0810042760455", "0810042760691"], "unii": ["L7T10EIP3A"], "rxcui": ["1148429"], "spl_set_id": ["f45eb95a-2813-4124-bdb0-54e078a8237d"], "manufacturer_name": ["REAL TIME PRODUCTS, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 TUBE (84573-517-03)", "package_ndc": "84573-517-03", "marketing_start_date": "20240712"}, {"sample": false, "description": "120 mL in 1 TUBE (84573-517-04)", "package_ndc": "84573-517-04", "marketing_start_date": "20240712"}, {"sample": false, "description": "147.8 mL in 1 TUBE (84573-517-05)", "package_ndc": "84573-517-05", "marketing_start_date": "20240712"}, {"sample": false, "description": "210 mL in 1 TUBE (84573-517-07)", "package_ndc": "84573-517-07", "marketing_start_date": "20240712"}, {"sample": false, "description": "354 mL in 1 TUBE (84573-517-12)", "package_ndc": "84573-517-12", "marketing_start_date": "20240712"}, {"sample": false, "description": "473 mL in 1 TUBE (84573-517-16)", "package_ndc": "84573-517-16", "marketing_start_date": "20240712"}, {"sample": false, "description": "1893 mL in 1 BOTTLE (84573-517-64)", "package_ndc": "84573-517-64", "marketing_start_date": "20240816"}], "brand_name": "Real Time Pain Relief Maxx Topical Analgesic", "product_id": "84573-517_2019e91f-7c9a-32bb-e063-6294a90ad6ba", "dosage_form": "LOTION", "product_ndc": "84573-517", "generic_name": "MENTHOL", "labeler_name": "REAL TIME PRODUCTS, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Real Time Pain Relief Maxx Topical Analgesic", "active_ingredients": [{"name": "MENTHOL", "strength": "15 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240712", "listing_expiration_date": "20261231"}