Uline Hand Sanitizer

Manufacturer
Uline | Betco Corporation, Ltd
Effective date
2026-08-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-08-08 02:01:16

Label at a glance#

ProductUline Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Uses • Hand sanitizer to reduce microorganisms on the skin. • Use this product when soap and water are not available.

Dosage and administration

Directions • Read the entire label before using this product. • Place enough product on your palm to thoroughly cover your hands. • Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70%

Uses

INDICATIONS & USAGE SECTION

Uses

• Hand sanitizer to reduce microorganisms on the skin.

• Use this product when soap and water are not available.

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Warnings

WARNINGS SECTION

Warnings

• For external use only.

• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

• FLAMMABLE. This product contains ethyl alcohol. Keep away from

sources of ignition.

• Discontinue use if irritation or redness develops.

• If irritation persists for more than 72 hours, consult a physician.

• KEEP OUT OF REACH OF CHILDREN.

• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

• Read the entire label before using this product.

• Place enough product on your palm to thoroughly cover your hands.

• Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, PEG/PPG-8/3 Laurate, Gycerin, Carbomer, Tetrahydroxypropylethylendiamine, Fragrance.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3780 ml label3780 ml label3780 ml 69790-801-04

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69790-80169790-801-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-11-18full-release2026-06-01 00:48:30

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
Uline Hand SanitizerALCOHOLUlinea7aa3bde-d36e-f9d4-e053-2a95a90a6e6a2026-08-06WarningsExact identifier
ndc (package): 69790-801-04
ndc (product): 69790-801
ndc11 (package): 69790080104
spl id: 5862330f-ec5f-1937-e063-6294a90a6c68
spl set id: a7aa3bde-d36e-f9d4-e053-2a95a90a6e6a

Reported adverse events (FAERS/openFDA)#

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