FDA.reportPublic FDA data

PURELL Advanced Foam Hand Rub

Manufacturer
GOJO Industries, Inc.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:50:18

Label at a glance#

ProductPURELL Advanced Foam Hand Rub
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 FoamPSN3
616805ethanol 0.7 ML/ML Topical FoamSCD3
616805ethanol 70 % Topical FoamSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-982-17PURELL Advanced Foam Hand Rub515 mL in 1 PACKAGELIQUID5153
21749-982-45PURELL Advanced Foam Hand Rub45 mL in 1 PACKAGELIQUID453
21749-982-53PURELL Advanced Foam Hand Rub535 mL in 1 PACKAGELIQUID5353
21749-982-89PURELL Advanced Foam Hand Rub1200 mL in 1 PACKAGELIQUID12003
21749-982-97PURELL Advanced Foam Hand Rub700 mL in 1 PACKAGELIQUID7003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-982PURELL ADVANCED FOAM HAND RUB (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]35 package rows20250101_f67dac52-88d9-4d46-84db-517b01acdcd9.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
21749-98221749-982-45, 21749-982-53, 21749-982-97, 21749-982-89, 21749-982-17

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
2a96b927-af65-db3c-e063-6394a90a05f8f67dac52-88d9-4d46-84db-517b01acdcd92024-12-31Exact identifier
spl id: 2a96b927-af65-db3c-e063-6394a90a05f8
spl set id: f67dac52-88d9-4d46-84db-517b01acdcd9

Reported adverse events (FAERS/openFDA)#

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