FDA.reportPublic FDA data

PURELL Antiseptic Hand Foam

Manufacturer
GOJO Industries, Inc.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:49:56

Label at a glance#

ProductPURELL Antiseptic Hand Foam
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN2
616805ethanol 0.7 ML/ML Topical FoamSCD2
616805ethanol 70 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-832-45PURELL Antiseptic Hand Foam45 mL in 1 PACKAGELIQUID452
21749-832-53PURELL Antiseptic Hand Foam535 mL in 1 PACKAGELIQUID5352
21749-832-89PURELL Antiseptic Hand Foam1200 mL in 1 PACKAGELIQUID12002
21749-832-90PURELL Antiseptic Hand Foam1250 mL in 1 PACKAGELIQUID12502
21749-832-97PURELL Antiseptic Hand Foam700 mL in 1 PACKAGELIQUID7002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-832PURELL ANTISEPTIC HAND FOAM (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]25 package rows20250101_53df2efd-b3be-4299-8130-f3c63beaef26.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-83221749-832-45, 21749-832-53, 21749-832-97, 21749-832-89, 21749-832-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

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
2a96e435-8e11-804d-e063-6394a90a5fad53df2efd-b3be-4299-8130-f3c63beaef262024-12-31Exact identifier
spl id: 2a96e435-8e11-804d-e063-6394a90a5fad
spl set id: 53df2efd-b3be-4299-8130-f3c63beaef26

Reported adverse events (FAERS/openFDA)#

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