Algonquin HanClean Foam

Manufacturer: Whisk Products, Inc.
Effective date: 2025-03-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:56:32

Label at a glance#

ProductAlgonquin HanClean Foam

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

Reduces amount of bacteria on hands Recommended for repeated use

Dosage and administration

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for fifteen seconds. Rinse with potable water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Reduces amount of bacteria on hands
Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of foam into palm of hand.
Rub thoroughly over all surfaces of both hands for fifteen seconds.
Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - 4 L Kwik-Klick Cartridge

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	PSN	1
1233282	benzalkonium chloride 1 MG/ML Medicated Liquid Soap	SCD	1
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
65585-530-01	Algonquin HanClean Foam	4000 mL in 1 BOTTLE, PUMP	SOLUTION	4000	1
65585-530-02	Algonquin HanClean Foam	1000 mL in 1 BAG	SOLUTION	1000	1
65585-530-02	Algonquin HanClean Foam	8 in 1 BOX	SOLUTION	8	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65585-530	ALGONQUIN HANCLEAN FOAM (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]	1	Current NDC, 3 package rows	20250305_2f73c3a7-426e-51f4-e063-6394a90aad4f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Algonquin HanClean Foam
Benzalkonium Chloride
BENZALKONIUM
WATER
LAURAMINE OXIDE
CITRIC ACID MONOHYDRATE
PHENOXYETHANOL
GLYCERIN
PEG-120 METHYL GLUCOSE DIOLEATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-530	65585-530-01, 65585-530-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
GLYCERIN	PDC6A3C0OX	IACT
PEG-120 METHYL GLUCOSE DIOLEATE	YM0K64F20V	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Algonquin HanClean Foam	BENZALKONIUM CHLORIDE	Whisk Products, Inc.	2f73c3a7-426e-51f4-e063-6394a90aad4f	2025-03-03	Warnings	Exact identifier ndc (package): 65585-530-02 ndc (package): 65585-530-01 ndc (product): 65585-530 ndc11 (package): 65585053002 ndc11 (package): 65585053001 spl id: 2f73c028-ce59-5a57-e063-6294a90a705a spl set id: 2f73c3a7-426e-51f4-e063-6394a90aad4f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.