Antibacterial

Manufacturer
Meijer, Inc. | Nice-Pak Products, LLC
Effective date
2026-02-20
Label type
HUMAN OTC DRUG LABEL
Version
19
Source
full-release
Hydrated at
2026-06-01 01:46:50

Label at a glance#

ProductAntibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Dosage and administration

Apply to wet hands, lather into rich foam and rinse well.

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

ANTIBACTERIAL

hand saop

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Apply to wet hands, lather into rich foam and rinse well.

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

  • if irritation and redness develop
  • comdition 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, 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

Disclaimer

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distribute by the Colgate-Palmolive Company, distributor of Softsoap Antibacterial Hand Soap White Tea & Berry.

Adverse reaction

ADVERSE REACTIONS SECTION

Questions 1-888-593-0593

DISTRIBUTED BY

MEIJER DISTRIBUTION, INC

GRAND RAPIDS, MI 49544

www.meijer.com

OUR QUALITY GUARANTEE

The Meijer Family

WWW.MEIJER.COM/SATISFACTION

Empty Before Recycling

PLASTIC BOTTLE

how2recycle.info

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

meijer ®

ANTIBACTERIAL

hand soap

BERRIES & WHITE TEA SCENT

CONTAINS MOISTURIZERS

PARABEN FREE & PHTHALATE FREE

Compare to Softsoap ®Hand Soap*

50 FL OZ (1.56 QT) 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 SoapPSN19
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD19
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY19
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY19

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-976-03Antibacterial1478 mL in 1 BOTTLE, PLASTICSOAP147819
41250-976-68Antibacterial1656 mL in 1 BOTTLE, PLASTICSOAP165619

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-97641250-976-68, 41250-976-03

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
AntibacterialBENZALKONIUM CHLORIDEMeijer, Inc.d450c423-00fa-4bb7-a0be-c14412a45e282026-02-20Warnings, Adverse reactionsExact identifier
ndc (package): 41250-976-68
ndc (package): 41250-976-03
ndc (product): 41250-976
ndc11 (package): 41250097668
ndc11 (package): 41250097603
spl id: 4b4429f9-f3d5-b9c1-e063-6294a90a415f
spl set id: d450c423-00fa-4bb7-a0be-c14412a45e28

Reported adverse events (FAERS/openFDA)#

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