PURELL Advanced Hand Sanitizer Fragrance Free

Manufacturer: GOJO Industries, Inc.
Effective date: 2026-03-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:51:50

Label at a glance#

ProductPURELL Advanced Hand Sanitizer Fragrance Free

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Reduces bacteria on the skin

Dosage and administration

Place product on hands Rub until dry

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

Reduces bacteria on the 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 product on hands
Rub until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
21749-532-01	PURELL Advanced Hand Sanitizer Fragrance Free	1.2 mL in 1 PACKET	LIQUID	1.2	1
21749-532-27	PURELL Advanced Hand Sanitizer Fragrance Free	800 mL in 1 BOTTLE	LIQUID	800	1
21749-532-40	PURELL Advanced Hand Sanitizer Fragrance Free	1200 mL in 1 BOTTLE	LIQUID	1200	1

Products#

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

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

PURELL Advanced Hand Sanitizer Fragrance Free
ALCOHOL
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)
WATER
ISOPROPYL ALCOHOL
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE, D-
CAPRYLYL GLYCOL
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
21749-532	21749-532-01, 21749-532-27, 21749-532-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)	8Z5ZAL5H3V	IACT
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
.ALPHA.-TOCOPHEROL ACETATE, D-	A7E6112E4N	IACT
CAPRYLYL GLYCOL	00YIU5438U	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PURELL Advanced Hand Sanitizer Fragrance Free	ALCOHOL	GOJO Industries, Inc.	4e06bb4a-e1a5-8c79-e063-6294a90a293c	2026-03-27	Warnings	Exact identifier ndc (package): 21749-532-01 ndc (package): 21749-532-27 ndc (package): 21749-532-40 ndc (product): 21749-532 ndc11 (package): 21749053201 ndc11 (package): 21749053240 ndc11 (package): 21749053227 spl id: 4e06bee4-c86e-bfdc-e063-6294a90afa2c spl set id: 4e06bb4a-e1a5-8c79-e063-6294a90a293c

Reported adverse events (FAERS/openFDA)#

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