PURELL Advanced Skin Balancing Hand Sanitizer

Manufacturer
GOJO Industries, Inc.
Effective date
2016-12-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:54:05

Label at a glance#

ProductPURELL Advanced Skin Balancing Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product.

Storage and handling

• Store below 110°F (43°C) • May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

• Store below 110°F (43°C) • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, Glycerin, Bacillus Ferment, Caprylyl Glycol, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-480-01PURELL Advanced Skin Balancing Hand Sanitizer30 mL in 1 BOTTLEGEL302
21749-480-02PURELL Advanced Skin Balancing Hand Sanitizer59 mL in 1 BOTTLEGEL592
21749-480-08PURELL Advanced Skin Balancing Hand Sanitizer236 mL in 1 BOTTLEGEL2362
21749-480-12PURELL Advanced Skin Balancing Hand Sanitizer354 mL in 1 BOTTLEGEL3542

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-480PURELL ADVANCED SKIN BALANCING HAND SANITIZER (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]2Legacy NDC, 4 package rows20180110_77c45065-549a-4132-9ae1-1f19ddf11bc0.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-48021749-480-01, 21749-480-02, 21749-480-08, 21749-480-12

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
d90acded-e708-4dfb-bd40-c60eb8e9435977c45065-549a-4132-9ae1-1f19ddf11bc02016-12-09WarningsExact identifier
spl id: d90acded-e708-4dfb-bd40-c60eb8e94359
spl set id: 77c45065-549a-4132-9ae1-1f19ddf11bc0

Reported adverse events (FAERS/openFDA)#

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