FDA.reportPublic FDA data

Meijer

Manufacturer
Meijer
Effective date
2025-03-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:58:06

Label at a glance#

ProductMeijer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

Helps eliminate bacteria on the skin

Dosage and administration

Dispense onto wet hand. 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

Uses

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on the skin

Warnings

WARNINGS SECTION

For external rectal use only

When using this product

OTC - WHEN USING SECTION

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

Stop using this product and ask a doctor it

OTC - ASK DOCTOR SECTION

irritation and redness develop and lasts

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 hand. Work into a lather. Rinse well

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Lauramidopropylamine Oxide, Myristamidopropylamine Oxide, PEG – 120 Methyl Glucose Dioleate, Cetrimonium Chloride, Glycerin, Citric Acid, Disodium EDTA, Fragrance, Methylisothiazolinone, Methylchloroisothiazolinone, Red 33 (CI17200), Blue 1 (CI42090)

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 79481-1013-2

Meijer ANTIBACTERIAL foaming handwash

GENTLE ENOUGH FOR EVERYDAY USE

32 FL OZ (1 QT)

LabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79481-1013-2Meijer946 mL in 1 BOTTLESOLUTION9463

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-1013MEIJER (BENZALKONIUM CHLORIDE) SOLUTION [MEIJER]3Current NDC, 1 package rows20250331_1e69a1b6-1b2b-8db7-e063-6294a90a78e9.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
79481-101379481-1013-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
WATER059QF0KO0RIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
EDETATE DISODIUM7FLD91C86KIACT

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
MeijerBENZALKONIUM CHLORIDEMeijer1e69a1b6-1b2b-8db7-e063-6294a90a78e92025-03-28WarningsExact identifier
ndc (package): 79481-1013-2
ndc (product): 79481-1013
ndc11 (package): 79481101302
spl id: 31696241-bac3-9128-e063-6294a90a069a
spl set id: 1e69a1b6-1b2b-8db7-e063-6294a90a78e9

Reported adverse events (FAERS/openFDA)#

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