Package 52000-038-25

{"route": ["TOPICAL"], "spl_id": "6af56e16-5a14-4a8b-9491-6891be500637", "openfda": {"upc": ["0676979555645"], "unii": ["L7T10EIP3A", "SOI2LOH54Z"], "rxcui": ["577232"], "spl_set_id": ["2a59a847-cc7a-42cf-b49a-92e7254c1629"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "283 g in 1 BOTTLE (52000-038-25)", "package_ndc": "52000-038-25", "marketing_start_date": "20171204"}, {"sample": false, "description": "226 g in 1 BOTTLE (52000-038-26)", "package_ndc": "52000-038-26", "marketing_start_date": "20171204"}], "brand_name": "Medicated Body", "product_id": "52000-038_6af56e16-5a14-4a8b-9491-6891be500637", "dosage_form": "POWDER", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "52000-038", "generic_name": "Menthol and Zinc Oxide", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medicated Body", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "1.5 mg/g"}, {"name": "ZINC OXIDE", "strength": "10 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}