Package 73062-032-01

Brand: inofoam antibacterial foaming hand wash

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 73062-032-01
Digits Only 7306203201
Product NDC 73062-032
Product ID 73062-032_0a59627b-cad3-b9b2-e063-6394a90a2f7f
Description

1 BOTTLE in 1 CARTON (73062-032-01) / 3800 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-11-20
Brand inofoam antibacterial foaming hand wash
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Inofoam Antibacterial Foaming Hand Wash ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0a59627b-cad3-b9b2-e063-6394a90a2f7f", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["4fc1e57f-b909-4dde-8c1a-2793af6eafb0"], "manufacturer_name": ["Avro Enterprises, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (73062-032-01)  / 3800 mL in 1 BOTTLE", "package_ndc": "73062-032-01", "marketing_start_date": "20231120"}], "brand_name": "Inofoam Antibacterial Foaming Hand Wash", "product_id": "73062-032_0a59627b-cad3-b9b2-e063-6394a90a2f7f", "dosage_form": "LIQUID", "product_ndc": "73062-032", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "Avro Enterprises, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Inofoam Antibacterial Foaming Hand Wash", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231120", "listing_expiration_date": "20261231"}