Foaming Hand

Manufacturer: Veritiv Operating Company | Nice-Pak Products, LLC
Effective date: 2026-02-16
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:46:03

Label at a glance#

ProductFoaming Hand

Active ingredientBENZALKONIUM CHLORIDE

Label structure12 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13 %

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands
apply palmful to hands
scrub thoroughly
rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

Claim

SPL UNCLASSIFIED SECTION

Product is NSF registered for use as a hand sanitizer in and around fool processing areas.

Adverse Reaction

ADVERSE REACTIONS SECTION

Distributed by: Vestis

1035 Alpharetta Street

Suite 2100

Roswell, GA 30075

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

vestis ^®

NSF

Nonfood Compounds Program Listed E2 157038

Antibacterial

E2 Sanitizing

Foaming Hand Soap

Fragrance Free

33.8 FL OZ (1.05 QT) 1 L

mm01mm02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	2
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	2
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	2
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	2

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0022322FA		mm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71897-224-86	Foaming Hand	1000 mL in 1 BOTTLE, PLASTIC	SOAP	1000		2

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Foaming Hand
Benzalkonium Chloride
LAURAMIDOPROPYLAMINE OXIDE
COCAMIDOPROPYL BETAINE
WATER
BENZALKONIUM
TETRASODIUM EDTA
CITRIC ACID
GLYCERIN
MYRISTAMIDOPROPYLAMINE OXIDE
LAURAMINE OXIDE
SODIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71897-224	71897-224-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LAURAMIDOPROPYLAMINE OXIDE	I6KX160QTV	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
TETRASODIUM EDTA	MP1J8420LU	IACT
CITRIC ACID	2968PHW8QP	IACT
GLYCERIN	PDC6A3C0OX	IACT
MYRISTAMIDOPROPYLAMINE OXIDE	3HSF539C9T	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
SODIUM BENZOATE	OJ245FE5EU	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
Foaming Hand	BENZALKONIUM CHLORIDE	Veritiv Operating Company	3b4dbfd0-f275-3502-e063-6294a90a8486	2026-02-16	Warnings, Adverse reactions	Exact identifier ndc (package): 71897-224-86 ndc (product): 71897-224 ndc11 (package): 71897022486 spl id: 4af5534d-3be0-730d-e063-6294a90a3eaf spl set id: 3b4dbfd0-f275-3502-e063-6294a90a8486

Reported adverse events (FAERS/openFDA)#

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