Package 12870-0001-1

{"route": ["TOPICAL"], "spl_id": "424dba13-53c3-5abf-e063-6394a90a4722", "openfda": {"unii": ["RU45X2JN0Z", "95IT3W8JZE"], "rxcui": ["1117536"], "spl_set_id": ["23b83457-8cbc-26f1-e054-00144ff8d46c"], "manufacturer_name": ["Arzol Chemical Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 PACKET in 1 BOX (12870-0001-1)  / 10 APPLICATOR in 1 PACKET / 100 mg in 1 APPLICATOR", "package_ndc": "12870-0001-1", "marketing_start_date": "19370101"}, {"sample": false, "description": "100 APPLICATOR in 1 VIAL (12870-0001-2)  / 100 mg in 1 APPLICATOR", "package_ndc": "12870-0001-2", "marketing_start_date": "19370101"}], "brand_name": "Silver Nitrate Applicators", "product_id": "12870-0001_424dba13-53c3-5abf-e063-6394a90a4722", "dosage_form": "STICK", "product_ndc": "12870-0001", "generic_name": "Silver Nitrate Applicators", "labeler_name": "Arzol Chemical Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Silver Nitrate Applicators", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "25 mg/100mg"}, {"name": "SILVER NITRATE", "strength": "75 mg/100mg"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19370101", "listing_expiration_date": "20261231"}