Hand Wipes

Manufacturer
Ningbo Alabama Trading LLC
Effective date
2020-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:32:10

Label at a glance#

ProductHand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

•  Thoroughly wipe hands with cloth •  Rub hands together until dry •  No rinsing required

Storage and handling

•  Dispose of properly, do not flush

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Use: • Hand sanitizer to help reduce bacteria on the skin. For use when soap and water not available.

WARNINGS SECTION

Warnings For external use only

When using this product

• Avoid getting into the eyes.

• In case of eye contact immediately flush eyes thoroughly with water.

Stop use and ask a doctor if

• Irritation or redness develops

• Condition persist for more than 72 hours

• Redness is present 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

• Thoroughly wipe hands with cloth

• Rub hands together until dry

• No rinsing required

Other information

STORAGE AND HANDLING SECTION

• Dispose of properly, do not flush

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water, polysorbate 20, glycerin, potassium sorbate, aloe (aloe barbadensis) leaf extract, dehydroacetic acid, phenoxyethanol citric acid.

SPL UNCLASSIFIED SECTION

SANITIZING

Cleanse on the Go

LEMON SCENTED WITH ALOE EXTRACT

KILLS 99.99% OF GERMS*

ALCOHOL FREE

*Kills 99.99% of most common germs that may cause illness.

Manufactured for 

Commonwealth Wholesale Corp

230 Central Ave

Teterboro, NJ 07608

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackagingPackagingPackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80408-619-032022-01-28C16284748780-1d6a99b39-e4a4-a426-e053-dadaa90af4c2HAND WIPES Cleanse on the Go

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80408-619-03Hand Wipes3.6 g in 1 PACKAGECLOTH3.61
80408-619-03Hand Wipes50 in 1 PACKETCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80408-619HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [NINGBO ALABAMA TRADING LLC]1Legacy NDC, 2 package rows20201021_bddbc4bd-61eb-4a00-8f3e-16bbc469f9cb.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80408-61980408-619-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
020d568a-3288-4972-9cac-6cb4107efa21bddbc4bd-61eb-4a00-8f3e-16bbc469f9cb2020-09-23WarningsExact identifier
spl id: 020d568a-3288-4972-9cac-6cb4107efa21
spl set id: bddbc4bd-61eb-4a00-8f3e-16bbc469f9cb

Reported adverse events (FAERS/openFDA)#

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