FDA.reportPublic FDA data

Benzalkonium Chloride

Manufacturer
Walmart Inc. | Nice-Pak Products, LLC
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:47:58

Label at a glance#

ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

  • Light, fresh scent
  • Formaldehyde donor-free
  • Paraben-free
  • Phthalate-free
  • Triclosan-free
  • Dermatologist tested
  • Helps kill harmful germs

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 conctact 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 rght away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

inactive ingredients

INACTIVE INGREDIENT SECTION

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, blue 1, red 33

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Satisfaction guaranteed - Or we'll replace it or give you your money back.  For questions or comments please call 1-888-287-1915.

DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716

*This product is not manufactured or distributed by the Colgate-Palmolive Company, owner of the registered trademark Softsoap ®.

Made in the USA with domestic and imported ingredients 

Factory Certified

how2recycle.info

Empty bottle before recycling

PLASTIC BOTTLE

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

equate™

NDC 79903-167-50

Compare to Softsoap ®Antibacterial Hand Soap White Tea & Berry Fusion* active ingredient

Berries & White Tea Scent

ANTIBACTERIAL HAND SOAP

DERMATIOLOGIST TESTED

With Moisturizers

Light, fresh scent

Helps kill harmful germs

FREE:

  • PARABEN
  • TRICLOSAN
  • PHTHALATE
  • FORMALDEHYDE DONOR

50 FL OZ (1 QT 1PT 2 FL OZ) 1.47 L

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN6
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD6
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY6
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-167-50Benzalkonium Chloride1470 mL in 1 BOTTLE, PLASTICGEL14706

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79903-16779903-167-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
SODIUM CHLORIDE451W47IQ8XIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
GLYCERINPDC6A3C0OXIACT
DISTEARETH-75 ISOPHORONE DIISOCYANATE5365FJ30SCIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
SULISOBENZONE1W6L629B4KIACT
SODIUM BENZOATEOJ245FE5EUIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-09-04legacy-cache2026-10-22 05:56:35

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Benzalkonium ChlorideBENZALKONIUM CHLORIDEWalmart Inc.99fba457-0eea-4c0b-987f-6a1690f503fb2026-02-27Warnings, Adverse reactionsExact identifier
ndc (package): 79903-167-50
ndc (product): 79903-167
ndc11 (package): 79903016750
spl id: 4bd556bf-02a2-1bce-e063-6294a90a7168
spl set id: 99fba457-0eea-4c0b-987f-6a1690f503fb

Reported adverse events (FAERS/openFDA)#

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