FDA.reportPublic FDA data

SCRUBS Hand Sanitizer Wipe

Manufacturer
ITW Pro Brands
Effective date
2023-09-28
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:25:29

Label at a glance#

ProductSCRUBS Hand Sanitizer Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

To decrease bacteria on the skin. Directions Wet hands thoroughly with product and allow to dry without wiping. Children under six years of age should be supervised when using this product

Dosage and administration

0.1% Antiseptic

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

•For hand washing to decrease bacteria on skin.

•Recommended for repeated use.

Warnings

WARNINGS SECTION

•do not get into eyes. If contact occurs rinse eyes thoroughly with water.

Flammable. Keep away from heat and flame.

FOR EXTERNAL USE ONLY

Ask your doctor

OTC - ASK DOCTOR SECTION

•If irritation arises and persists for more than 72 hours.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Keep out of the reach of children

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

SD Alcohol 40B

Mineral Oil

Isopropyl myristate

C11-15 Alketh-5

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

0.1%

Antiseptic

Indications and Usage

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Children under six years of age should be supervised when using this product

RECENT MAJOR CHANGES SECTION

Corrected Dosage & Administration section as it contained use directions rather than dosage value.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scrubs Hand Sanitizer - 85ctScrubs Hand Sanitizer - 85ct

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51239-190951239-1909-1, 51239-1909-2, 51239-1909-3

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
MINERAL OILT5L8T28FGPIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALCOHOL3K9958V90MIACT
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
0670d211-3374-ddbd-e063-6394a90aee2963b33bbf-d685-cf85-e053-2991aa0aa5282023-09-28WarningsExact identifier
spl id: 0670d211-3374-ddbd-e063-6394a90aee29
spl set id: 63b33bbf-d685-cf85-e053-2991aa0aa528

Reported adverse events (FAERS/openFDA)#

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