FDA.reportPublic FDA data

SCRUBS Hand Sanitizer Wipes

Manufacturer
ITW Pro Brands
Effective date
2024-02-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:08:53

Label at a glance#

ProductSCRUBS Hand Sanitizer Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Purpose

OTC - PURPOSE SECTION

PurposePurpose

Warnings

WARNINGS SECTION

WarningsWarnings

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask DoctorAsk Doctor

KOROC

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KOROCKOROC

Inactive Ingredients

INACTIVE INGREDIENT SECTION

InactivesInactives

Dosage

DOSAGE & ADMINISTRATION SECTION

DirectionsDirectionsDosageDosage

Uses

INDICATIONS & USAGE SECTION

UsesUses

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Full LabelFull Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN3
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD3
1038856benzalkonium chloride 0.1 % Medicated WipesSY3
1038856benzalkonium chloride 0.1 % Topical SwabSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51239-2909-12024-01-30C16284748780-11030e364-f9af-111a-e063-dadaa90a10e2SCRUBS Hand Sanitizer Wipes
51239-2909-22024-01-30C16284748780-11030e364-f9af-111a-e063-dadaa90a10e2SCRUBS Hand Sanitizer Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51239-2909-1SCRUBS Hand Sanitizer Wipes400 g in 1 CANISTERCLOTH4003
51239-2909-2SCRUBS Hand Sanitizer Wipes6 in 1 BOXCLOTH63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51239-2909SCRUBS HAND SANITIZER WIPES (BENZALKONIUM CHLORIDE) CLOTH [ITW PRO BRANDS]3Current NDC, 2 package rows20240224_067022d1-8ecd-a6ba-e063-6394a90a40f0.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51239-290951239-2909-1, 51239-2909-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINERAL OILT5L8T28FGPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
C11-15 PARETH-59G5POA2F31IACT

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
SCRUBS Hand Sanitizer WipesBENZALKONIUM CHLORIDEITW Pro Brands067022d1-8ecd-a6ba-e063-6394a90a40f02024-02-22WarningsExact identifier
ndc (package): 51239-2909-2
ndc (package): 51239-2909-1
ndc (product): 51239-2909
ndc11 (package): 51239290902
ndc11 (package): 51239290901
spl id: 11fa76e0-aaca-0ded-e063-6294a90a859e
spl set id: 067022d1-8ecd-a6ba-e063-6394a90a40f0

Reported adverse events (FAERS/openFDA)#

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