Lemon SCRUBS Hand Sanitizer Wipe

Manufacturer
ITW Pro Brands
Effective date
2023-06-19
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:29:47

Label at a glance#

ProductLemon SCRUBS Hand Sanitizer Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

•For hand washing to decrease bacteria on skin. •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.

Warning

WARNINGS SECTION

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

Flamable. Keep away from heat and flalme.

FOR EXTERNAL USE ONLY

Ask your doctor

OTC - ASK DOCTOR SECTION

Stop and ask a doctor

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

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.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

0.1%

Antiseptic

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

SD Alcohol 40B

Mineral Oil

Isopropyl Myristate

C11-15 Alketh-5

Perfume

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Indications and Usage

INDICATIONS & USAGE SECTION

•For hand washing to decrease bacteria on skin.

•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 erroneously included use directions.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Scrubs Lemon Hand Sanitizer - 120ctScrubs Lemon Hand Sanitizer - 120ct

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
51239-292951239-2929-1, 51239-2929-2, 51239-2929-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
fe81eaa4-6b21-6caf-e053-6394a90a6da563b018c5-005f-870f-e053-2991aa0a49662023-06-19WarningsExact identifier
spl id: fe81eaa4-6b21-6caf-e053-6394a90a6da5
spl set id: 63b018c5-005f-870f-e053-2991aa0a4966

Reported adverse events (FAERS/openFDA)#

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