Package 44224-1103-2

{"route": ["TOPICAL"], "spl_id": "4640051b-84fe-66c7-e063-6294a90a552e", "openfda": {"upc": ["0044224610300"], "unii": ["8MDF5V39QO"], "rxcui": ["1547234"], "spl_set_id": ["223d1de8-7940-bbdc-e063-6294a90a51d8"], "manufacturer_name": ["Tender Corporation d/b/a Adventure Ready Brands"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (44224-1103-2)  / 1 g in 1 VIAL (44224-1103-0)", "package_ndc": "44224-1103-2", "marketing_start_date": "20250617"}, {"sample": false, "description": "3 VIAL in 1 BOX (44224-1103-3)  / 14 g in 1 VIAL", "package_ndc": "44224-1103-3", "marketing_start_date": "20251218"}], "brand_name": "After Bite Advanced", "product_id": "44224-1103_4640051b-84fe-66c7-e063-6294a90a552e", "dosage_form": "LIQUID", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "44224-1103", "generic_name": "Sodium Bicarbonate", "labeler_name": "Tender Corporation d/b/a Adventure Ready Brands", "product_type": "HUMAN OTC DRUG", "brand_name_base": "After Bite Advanced", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": ".7 g/14g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}