PURELL Green Certified Instant Hand Sanitizer Foam (ETHYL ALCOHOL)

Manufacturer
GOJO Industries, Inc.
Effective date
2021-03-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:47:11

Label at a glance#

ProductPURELL Green Certified Instant Hand Sanitizer Foam (ETHYL ALCOHOL)
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease Recommended for repeated use

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry Children under 6 years of age should be supervised when using PURELL

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product in your palm to cover hands and rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using PURELL

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, PEG-10 Dimethicone, Glycerin, Hydroxyethyl Urea, Isopropyl Myristate, PEG-12 Dimethicone, Propylene Glycol, Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct LabelProduct LabelProduct LabelProduct LabelProduct Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M3
ALCOHOLACTIVE MOIETY3K9958V90M3

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-98721749-987-53, 21749-987-51, 21749-987-97, 21749-987-10, 21749-987-89

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 · Source PDF

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
796ad152-9e0e-43bb-95ba-f35c913855775b9191e0-da0f-47e6-9d8a-5cd6637bd2b32021-03-29WarningsExact identifier
spl id: 796ad152-9e0e-43bb-95ba-f35c91385577
spl set id: 5b9191e0-da0f-47e6-9d8a-5cd6637bd2b3

Reported adverse events (FAERS/openFDA)#

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