Package 69993-044-01

{"route": ["TOPICAL"], "spl_id": "30b85890-e72d-4af7-bda9-e7744abc92af", "openfda": {"nui": ["N0000175682", "M0000897", "N0000175426", "N0000175976"], "upc": ["0045611016088"], "unii": ["98PI200987"], "spl_set_id": ["30b85890-e72d-4af7-bda9-e7744abc92af"], "pharm_class_cs": ["Amides [CS]"], "pharm_class_pe": ["Local Anesthesia [PE]"], "pharm_class_epc": ["Amide Local Anesthetic [EPC]", "Antiarrhythmic [EPC]"], "manufacturer_name": ["Kingsway Pharmaceuticals dba NFI, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69993-044-01)  / 28 g in 1 TUBE", "package_ndc": "69993-044-01", "marketing_start_date": "20250901"}], "brand_name": "Bikini Zone Medicated Gel", "product_id": "69993-044_30b85890-e72d-4af7-bda9-e7744abc92af", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "69993-044", "generic_name": "Lidocaine", "labeler_name": "Kingsway Pharmaceuticals dba NFI, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bikini Zone Medicated Gel", "active_ingredients": [{"name": "LIDOCAINE", "strength": "2 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}