PURELL Foaming Hand Sanitizer

Manufacturer
GOJO Industries, Inc.
Effective date
2005-07-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:14:19

Label at a glance#

ProductPURELL Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

• Place 3g of PURELL® product in your palm and thoroughly cover hands, including between fingers, under fingernails, and around wrists. • Rub briskly until dry. • No rinsing required. • Children under 6 years of age should be supervised when using this product.

Storage and handling

May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.5%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

• Hand sanitizer to help reduce bacteria on the skin that could cause disease

• Recommended for repeated use

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only 

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

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.

OTHER SAFETY INFORMATION

Contents under pressure. Do not puncture or incinerate container. Do not store at temperature above 120°F (48°C).

Directions

DOSAGE & ADMINISTRATION SECTION

• Place 3g of PURELL® product in your palm and thoroughly cover hands, including between fingers, under fingernails, and around wrists.

• Rub briskly until dry.

• No rinsing required.

• Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Hydrofluorocarbon 152a, Isobutane, Emulsifying Wax NF, Cetyl Lactate, Steareth-2, Propane, Sodium Benzoate, Sodium Sesquicarbonate, Fragrance (Parfum)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product labelProduct label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-10021749-100-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
868aa0f5-4e68-412f-96c0-7b14fce47578ffc656d2-9361-4a61-a917-ce348ff83fb72022-11-16WarningsExact identifier
spl set id: ffc656d2-9361-4a61-a917-ce348ff83fb7

Reported adverse events (FAERS/openFDA)#

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