Hand Sanitizer

Manufacturer
Office Max | Consumer Product Partners, LLC
Effective date
2024-09-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:54:28

Label at a glance#

ProductHand Sanitizer Fragrance Free
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

To decrease bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

FLAMMABLE, keep away from fire and flame

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes   

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops.  If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek immediate medical attention or call a poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Caprylic/Capric Triglyceride, Isopropyl Myristate

Additional rear label text for manual dispensers

SPL UNCLASSIFIED SECTION

HighMark Manual Dispenser Foam Hand Sanitzer Refill

Distributed by: Office Depot, LLC

6600 N. Military Trail, Boca Raton, FL 33496 USA

Highmark is a trademark or registered trademark of OMX, Inc.

@2020 Office Depot, LLC.  All Rights Reserved.

Made in USA with foreign and domestic materials

Manufactured for Georgia-Pacific Consumer Products LP, Atlanta, GA 30303

Questions? Call 1-877-674-0688

Alcohol permit SDS-MO-15036  DSP-MO-28 DSP-MO-34

33.9 FL OZ (1000 mL)

Additional rear label text for automatic dispensers

SPL UNCLASSIFIED SECTION

HighMark Automatic Dispenser Foam Hand Sanitzer Refill

Distributed by: Office Depot, LLC

6600 N. Military Trail, Boca Raton, FL 33496 USA

Highmark is a trademark or registered trademark of OMX, Inc.

@2020 Office Depot, LLC. All Rights Reserved.

Made in USA with foreign and domestic materials

Manufactured for Georgia-Pacific Consumer Products LP, Atlanta, GA 30303

Questions? Call 1-877-674-0688

Alcohol permit SDS-MO-15036 DSP-MO-28 DSP-MO-34

33.9 FL OZ (1000 mL)

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MANUAL DISPENSER REFILL

FOAM HAND SANITIZER

FRAGRANCE FREE

33.9 fl oz (1000 mL)

image descriptionimage description

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AUTOMATED DISPENSER REFILL

FOAM HAND SANITIZER

FRAGRANCE FREE

33.9 FL OZ (1000 mL)

image descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61139-701HAND SANITIZER FRAGRANCE FREE (ETHYL ALCOHOL) SOLUTION [OFFICE MAX]6Legacy NDC20240922_b13d346d-ef57-4123-af19-1fcdd7bb1b9f.zip

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
61139-70161139-701-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
3bdc082c-4a1c-5c83-e063-6394a90a06b7b13d346d-ef57-4123-af19-1fcdd7bb1b9f2025-08-08WarningsExact identifier
spl set id: b13d346d-ef57-4123-af19-1fcdd7bb1b9f

Reported adverse events (FAERS/openFDA)#

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