foaming hand

Generic: benzalkonium chloride

Labeler: veritiv operating company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foaming hand
Generic Name benzalkonium chloride
Labeler veritiv operating company
Dosage Form SOAP
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1.3 mg/mL

Manufacturer
Veritiv Operating Company

Identifiers & Regulatory

Product NDC 71897-224
Product ID 71897-224_4af5534d-3be0-730d-e063-6294a90a3eaf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2025-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71897224
Hyphenated Format 71897-224

Supplemental Identifiers

RxCUI
1046593
UNII
F5UM2KM3W7

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name foaming hand (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.3 mg/mL
source: ndc
Packaging
  • 1000 mL in 1 BOTTLE, PLASTIC (71897-224-86)
source: ndc

Packages (1)

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

Ingredients (1)

benzalkonium chloride (1.3 mg/mL)

Linked Drug Pages (1)

Foaming Hand ndc-match (0.9)

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"}