Algonquin HanClean Foam

Manufacturer: Whisk Products, Inc.
Effective date: 2020-05-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:33:09

Label at a glance#

ProductAlgonquin HanClean Foam

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

For hand washing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Pump a small amout 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 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin
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 amout 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, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4 L Bottle

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1046593	Benzalkonium (Soap)	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD Active
1020365	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD Active

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Algonquin HanClean Foam
Benzalkonium Chloride
BENZALKONIUM
WATER
COCO GLUCOSIDE
LAURTRIMONIUM CHLORIDE
COCAMIDOPROPYLAMINE OXIDE
CITRIC ACID MONOHYDRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-518	65585-518-01, 65585-518-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
COCO GLUCOSIDE	ICS790225B	IACT
LAURTRIMONIUM CHLORIDE	A81MSI0FIC	IACT
COCAMIDOPROPYLAMINE OXIDE	M4SL82J7HK	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
b019e7ee-ce4d-4eaf-9c0c-c34956922897			fd4640c4-e570-4ee3-9e39-711d24811761	2020-05-01	Warnings	Exact identifier spl id: b019e7ee-ce4d-4eaf-9c0c-c34956922897 spl set id: fd4640c4-e570-4ee3-9e39-711d24811761

Reported adverse events (FAERS/openFDA)#

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