Hand Wash

Manufacturer: Walmart Inc. | Nice-Pak Products, LLC
Effective date: 2026-02-17
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:46:00

Label at a glance#

ProductHand Wash

Active ingredientBENZALKONIUM CHLORIDE

Label structure11 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Contacts and useful links#

PhoneLabel contact1-888-287-1915

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

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, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, blue 1, red 33

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed by: Walmart Inc.,

Bentonville, AR 72716

Information: 1-888-287-1915 or Walmart.com/help

Made in the USA with domestic and imported ingredients

Factory Certified

PLASTIC JUG

Widely Recyclable

Discard Seal, Empty & Replace Cap

how2recycle.info

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VALUE SIZE

NDC 79903-163-08

equate ^™

Fresh Scent

FOAMING HAND WASH

ANTIBACTERIAL

Helps kill harmful germs
Gentle and mild formula

PARABEN, TRICLOSAN, PHTHALATE FREE

128 FL OZ (1 GAL) 3.79 L

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	7
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	7
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	7
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	7

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0021733SB		mm01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79903-163-08	Hand Wash	3785 mL in 1 BOTTLE, PLASTIC	LIQUID	3785	7
79903-163-32	Hand Wash	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	7
79903-163-96	Hand Wash	221 mL in 1 BOTTLE, PLASTIC	LIQUID	221	7

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Hand Wash
Benzalkonium chloride
WATER
COCAMIDOPROPYL BETAINE
LAURAMIDOPROPYLAMINE OXIDE
LAURAMINE OXIDE
MYRISTAMIDOPROPYLAMINE OXIDE
GLYCERIN
CITRIC ACID MONOHYDRATE
EDETATE SODIUM
SULISOBENZONE
SODIUM BENZOATE
FD&C BLUE NO. 1
D&C RED NO. 33
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79903-163	79903-163-32, 79903-163-08, 79903-163-96

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
LAURAMIDOPROPYLAMINE OXIDE	I6KX160QTV	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
MYRISTAMIDOPROPYLAMINE OXIDE	3HSF539C9T	IACT
GLYCERIN	PDC6A3C0OX	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
EDETATE SODIUM	MP1J8420LU	IACT
SULISOBENZONE	1W6L629B4K	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Hand Wash	BENZALKONIUM CHLORIDE	Walmart Inc.	25d227f8-2238-4f6f-aa40-b314d0179d88	2026-02-17	Warnings, Adverse reactions	Exact identifier ndc (package): 79903-163-96 ndc (package): 79903-163-08 ndc (package): 79903-163-32 ndc (product): 79903-163 ndc11 (package): 79903016332 ndc11 (package): 79903016308 ndc11 (package): 79903016396 spl id: 4b05d712-0646-ed7f-e063-6294a90abb2e spl set id: 25d227f8-2238-4f6f-aa40-b314d0179d88

Reported adverse events (FAERS/openFDA)#

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