Package 37808-919-12

{"route": ["TOPICAL"], "spl_id": "2489f87a-061e-c0c7-e063-6394a90ad386", "openfda": {"upc": ["0041220721986"], "unii": ["G63QQF2NOX", "V06SV4M95S", "4X49Y0596W", "5A68WGF6WM"], "spl_set_id": ["b9a9837a-094b-4a57-a50c-5c1437deda7b"], "manufacturer_name": ["H.E.B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 TUBE (37808-919-12)", "package_ndc": "37808-919-12", "marketing_start_date": "20190206"}], "brand_name": "H.E.B BANANA", "product_id": "37808-919_2489f87a-061e-c0c7-e063-6394a90ad386", "dosage_form": "LOTION", "product_ndc": "37808-919", "generic_name": "SPF 50 Sunscreen", "labeler_name": "H.E.B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "H.E.B BANANA", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/mL"}, {"name": "HOMOSALATE", "strength": "100 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190206", "listing_expiration_date": "20261231"}