FDA.reportPublic FDA data

SCRUBS Hand Sanitizer Towelette

Manufacturer
ITW Pro Brands | Celeste Industries Corporation
Effective date
2020-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:06:53

Label at a glance#

ProductSCRUBS Hand Sanitizer Towelette
Active ingredientBenzalkonium Chloride
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Apply to hands Allow skin to dry without wiping

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to hands
  • Allow skin to dry without wiping

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Ethyl Alcohol, Cocamidopropyl PG-Dimonium Chloride Phosphate, Linear alcohol ethoxylate, Fragrance

PRINCIPAL DISPLAY PANEL - 1.75 mL Towelette Pouch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SCRUBS®

HAND
SANITIZER
TOWELETTE

  • Kills 99.9% of Germs
  • Conditions & Moisturizes Skin
  • Antibacterial

CONTAINS:
1 PRE-MOISTENED TOWELETTE
8" x 5.5" (20.3 cm x 13.9 cm)

1.75 mL

PRINCIPAL DISPLAY PANEL - 1.75 mL Towelette Pouch
PRINCIPAL DISPLAY PANEL - 1.75 mL Towelette Pouch

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51239-094951239-0949-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
C9-11 PARETH-6KCE0V8JT7WIACT

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
eff77a14-65b9-2c65-e053-2995a90acf4d7e000cb0-21de-4035-90a4-25b0331b28912022-12-16WarningsExact identifier
spl set id: 7e000cb0-21de-4035-90a4-25b0331b2891

Reported adverse events (FAERS/openFDA)#

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