FDA.reportPublic FDA data

Meijer Antibacterial Foaming Hand Wash

Manufacturer
Meijer, Inc.
Effective date
2025-03-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:58:22

Label at a glance#

ProductMeijer Antibacterial Foaming Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Dispense onto wet hands. Work into a lather. Rinse well.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop using this product and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop and last

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion get medical help or contact Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Dispense onto wet hands. Work into a lather. Rinse well.

Other Information

SPL UNCLASSIFIED SECTION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Lauramidopropylamine Oxide, Myristamidopropylamine Oxide, PEG - 120, Methyl Glucose Dioleate,Cetrimonium Chloride, Glycerin, Citric Acid, Disodium EDTA, Frag rance, Methylisothiazolinone, Methylchloroisothiazolinone, Blue i(CI42090), Red 33(CI17200)

Questions or Comments?

OTC - QUESTIONS SECTION

Call toll free 1-800-527-7731

DISTRIBUTED BY

SPL UNCLASSIFIED SECTION

MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544. www.meijer.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC Code: 79481-1020-8

meijer

ANTIBACTERIAL Foaming Hand Soap

GENTLE ENOUGH FOR EVERYDAY USE

7.5 FL OZ. (221.8ML)

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-1020-8Meijer Antibacterial Foaming Hand Wash221.8 mL in 1 BOTTLE, PUMPSOAP221.83

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-1020MEIJER ANTIBACTERIAL FOAMING HAND WASH (0.13% BENZALKONIUM CHLORIDE SOLUTION) SOAP [MEIJER, INC.]3Current NDC, 1 package rows20250403_1eb6b603-ef96-dfda-e063-6294a90ae468.zip

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
79481-102079481-1020-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
WATER059QF0KO0RIACT
POLYETHYLENE GLYCOL 600030IQX730WEIACT
METHYL GLUCOSE DIOLEATEFA9KFJ4Z6PIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE DISODIUM7FLD91C86KIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
GLYCERINPDC6A3C0OXIACT
D&C RED NO. 339DBA0SBB0LIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT

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
Meijer Antibacterial Foaming Hand Wash0.13% BENZALKONIUM CHLORIDE SOLUTIONMeijer, Inc.1eb6b603-ef96-dfda-e063-6294a90ae4682025-03-31WarningsExact identifier
ndc (package): 79481-1020-8
ndc (product): 79481-1020
ndc11 (package): 79481102008
spl id: 31ab7f63-2c04-b319-e063-6294a90a2d05
spl set id: 1eb6b603-ef96-dfda-e063-6294a90ae468

Reported adverse events (FAERS/openFDA)#

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