Package 71513-202-31

{"route": ["TOPICAL"], "spl_id": "43cc182d-40d2-0cf5-e063-6394a90a2736", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1020364"], "spl_set_id": ["d4b3f6cf-52d3-1755-e053-2a95a90a9482"], "manufacturer_name": ["Broder Bros Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (71513-202-30)", "package_ndc": "71513-202-30", "marketing_start_date": "20251117"}, {"sample": false, "description": "20 mL in 1 BOTTLE (71513-202-31)", "package_ndc": "71513-202-31", "marketing_start_date": "20251117"}], "brand_name": "Antibacterial Hand Sanitizer", "product_id": "71513-202_43cc182d-40d2-0cf5-e063-6394a90a2736", "dosage_form": "SPRAY", "product_ndc": "71513-202", "generic_name": "Ethyl Alcohol", "labeler_name": "Broder Bros Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Antibacterial Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251117", "listing_expiration_date": "20261231"}