FDA.reportPublic FDA data

Benzalkonium Chloride

Manufacturer
Wal-Mart Stores, Inc. | Vi-Jon, LLC
Effective date
2022-12-06
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:45:16

Label at a glance#

ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

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 ingredients

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

Stop use and ask a doctore 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

Direction

DOSAGE & ADMINISTRATION SECTION

  • wet hands
  • apply palmful to hands
  • scrub thorought 
  • 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

claims

ADVERSE REACTIONS SECTION

Satisfaction guaranteed - Or we'll refplace 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

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

equate

NDC 79903-097-03

Compare to Softsoap Antibacterial Hand Soap White Tea & Berry Fusion

Berries & White Tea Scent

ANTIBACTERIAL HAND SOAP

DERMATIOLOGIST TESTED

With Moisturizers

Light, fresh scent

Helps kill harmful germs

PARABEN

TRICLOSAN

PHTHALATE

FORMALDEHYDE DONER

FREE

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

image descriptionimage description

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
79903-09779903-097-03

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2488619c-2e19-6c19-e063-6394a90a44d24ddf246c-6d95-4232-b2e3-1a3c26bee4332024-10-15Warnings, Adverse reactionsExact identifier
spl set id: 4ddf246c-6d95-4232-b2e3-1a3c26bee433

Reported adverse events (FAERS/openFDA)#

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