PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam

Manufacturer
GOJO Industries, Inc. | Travis Association for the Blind
Effective date
2024-12-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:42:26

Label at a glance#

ProductPURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

• Place enough product in your palm to thoroughly cover your hands • Rub hands together briskly until dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

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 productdo 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 ifirritation 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Avena Sativa (Oat) Kernel Extract, Canarium Luzonicum Gum Nonvolatiles, Caprylyl glycol, Citrus Aurantifolia (Lime) Peel Oil, Citrus Aurantium Bergamia (Bergamot) Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Glycerin, Isopropyl Myristate, Litsea Cubeba Fruit Oil, Mentha Arvensis Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Niaciniamide, Pinus Silvestrus Leaf Oil, Pogostemon Cablin Oil, PPG-12/SMDI copolymer, Schinus Molle Oil, Tocopheryl Acetate, Potassium Sorbate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN4
616805ethanol 0.7 ML/ML Topical FoamSCD4
616805ethanol 70 % Topical FoamSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-854-53PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam535 mL in 1 BOTTLELIQUID5354
21749-854-89PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam1200 mL in 1 BOTTLELIQUID12004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-854PURELL HEALTHCARE ADVANCED HAND SANITIZER ULTRA NOURISHING FOAM (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]4Current NDC, Legacy NDC, 2 package rows20241213_4fa85619-257f-4a19-a8f2-5a2e4b809726.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-85421749-854-53, 21749-854-89

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING FoamALCOHOLGOJO Industries, Inc.4fa85619-257f-4a19-a8f2-5a2e4b8097262024-12-11WarningsExact identifier
ndc (package): 21749-854-53
ndc (package): 21749-854-89
ndc (product): 21749-854
ndc11 (package): 21749085453
ndc11 (package): 21749085489
spl id: 2905d739-8b51-5773-e063-6394a90a5b63
spl set id: 4fa85619-257f-4a19-a8f2-5a2e4b809726

Reported adverse events (FAERS/openFDA)#

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