foaming advanced antibacterial hand

Generic: benzalkonium chloride

Labeler: kutol products company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foaming advanced antibacterial hand
Generic Name benzalkonium chloride
Labeler kutol products company
Dosage Form SOAP
Routes
TOPICAL
Active Ingredients

benzalkonium chloride .003 mg/mL

Manufacturer
Kutol Products Company

Identifiers & Regulatory

Product NDC 50865-213
Product ID 50865-213_298e23fa-a68d-383f-e063-6294a90a2e34
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50865213
Hyphenated Format 50865-213

Supplemental Identifiers

UPC
0686702213094
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 advanced antibacterial hand (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .003 mg/mL
source: ndc
Packaging
  • 3785 mL in 1 BOTTLE, PLASTIC (50865-213-13)
  • 50 mL in 1 BOTTLE, PLASTIC (50865-213-17)
  • 1000 mL in 1 BAG (50865-213-41)
  • 1200 mL in 1 BAG (50865-213-50)
  • 1000 mL in 1 BOTTLE, PLASTIC (50865-213-52)
  • 950 mL in 1 BOTTLE, PLASTIC (50865-213-78)
source: ndc

Packages (6)

Ingredients (1)

benzalkonium chloride (.003 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "298e23fa-a68d-383f-e063-6294a90a2e34", "openfda": {"upc": ["0686702213094"], "unii": ["F5UM2KM3W7"], "spl_set_id": ["7abc56b5-4446-4464-9b94-6c55f8bb9b74"], "manufacturer_name": ["Kutol Products Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (50865-213-13)", "package_ndc": "50865-213-13", "marketing_start_date": "20151001"}, {"sample": false, "description": "50 mL in 1 BOTTLE, PLASTIC (50865-213-17)", "package_ndc": "50865-213-17", "marketing_start_date": "20151001"}, {"sample": false, "description": "1000 mL in 1 BAG (50865-213-41)", "package_ndc": "50865-213-41", "marketing_start_date": "20151001"}, {"sample": false, "description": "1200 mL in 1 BAG (50865-213-50)", "package_ndc": "50865-213-50", "marketing_start_date": "20151001"}, {"sample": false, "description": "1000 mL in 1 BOTTLE, PLASTIC (50865-213-52)", "package_ndc": "50865-213-52", "marketing_start_date": "20151001"}, {"sample": false, "description": "950 mL in 1 BOTTLE, PLASTIC (50865-213-78)", "package_ndc": "50865-213-78", "marketing_start_date": "20151001"}], "brand_name": "Foaming Advanced Antibacterial Hand", "product_id": "50865-213_298e23fa-a68d-383f-e063-6294a90a2e34", "dosage_form": "SOAP", "product_ndc": "50865-213", "generic_name": "benzalkonium chloride", "labeler_name": "Kutol Products Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foaming Advanced Antibacterial Hand", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".003 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}