Antibacterial

Manufacturer
Sam's West, Inc. | Korex Chicago LLC
Effective date
2024-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:49:38

Label at a glance#

ProductAntibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

• Wet hands • Apply 5mL (teaspoonful) or palmful to hands and forearms • Rub vigorously for 20 seconds • Wash between fingers, around fingernails and backs of hands • Rinse thoroughly with warm water • Dry with paper towels or air-dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antiseptic Handwash

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use • In eyes

OTC - WHEN USING SECTION

When using this product

  • If in eyes, rinse promptly and thoroughly with water
  • Discontinue use if irritation and redness develop

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Skin irritation or redness occurs for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands • Apply 5mL (teaspoonful) or palmful to hands and forearms • Rub vigorously for 20 seconds • Wash between fingers, around fingernails and backs of hands • Rinse thoroughly with warm water • Dry with paper towels or air-dry

Other information

OTHER SAFETY INFORMATION

• For additional information, see Safety Data Sheet (SDS) • For emergency medical information, call 1-866-767-5045

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium chloride, Lauramine oxide, Cocamide MIPA, Lauramidopropylamine oxide, Sodium benzoate, PEG-120 methyl glucose dioleate, Citric acid, Glycerin, Sodium chloride, Fragrance, Disodium EDTA, Red 40.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68196-665-01

1

GALLON

M

Member's

Mark™

ANTIBACTERIAL

HAND SOAP

COMMERCIAL GRADE

KILLS 99.9% OF GERMS*

FRESH CLEAN FRAGRANCE

NET CONTENTS 1 GALLON (3.78 L)

container labelcontainer labelcontainer labelcontainer labelcontainer labelcontainer labelcontainer labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68196-665-01Antibacterial3.785 mL in 1 BOTTLE, PLASTICSOLUTION3.7851
68196-665-04Antibacterial3.78 mL in 1 BOTTLE, PLASTICSOLUTION3.781
68196-665-04Antibacterial4 in 1 CARTONSOLUTION41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68196-665ANTIBACTERIAL (BENZALKONIUM CHLORIDE) SOLUTION [SAM'S WEST, INC.]13 package rows20250101_2862f195-749e-c1b7-e063-6394a90ab214.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68196-66568196-665-01, 68196-665-04

Ingredients#

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

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

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
2862f195-749f-c1b7-e063-6394a90ab2142862f195-749e-c1b7-e063-6394a90ab2142024-12-03WarningsExact identifier
spl id: 2862f195-749f-c1b7-e063-6394a90ab214
spl set id: 2862f195-749e-c1b7-e063-6394a90ab214

Reported adverse events (FAERS/openFDA)#

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