Package 71897-224-86

Brand: foaming hand

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 71897-224-86
Digits Only 7189722486
Product NDC 71897-224
Product ID 71897-224_4af5534d-3be0-730d-e063-6294a90a3eaf
Description

1000 mL in 1 BOTTLE, PLASTIC (71897-224-86)

Marketing

Marketing Status
Marketed Since 2025-08-01
Brand foaming hand
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Foaming Hand ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4af5534d-3be0-730d-e063-6294a90a3eaf", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["3b4dbfd0-f275-3502-e063-6294a90a8486"], "manufacturer_name": ["Veritiv Operating Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (71897-224-86)", "package_ndc": "71897-224-86", "marketing_start_date": "20250801"}], "brand_name": "Foaming Hand", "product_id": "71897-224_4af5534d-3be0-730d-e063-6294a90a3eaf", "dosage_form": "SOAP", "product_ndc": "71897-224", "generic_name": "Benzalkonium Chloride", "labeler_name": "Veritiv Operating Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foaming Hand", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250801", "listing_expiration_date": "20271231"}