FDA.reportPublic FDA data

PURELL Advanced Hand Sanitizer Foam

Manufacturer
GOJO Industries, Inc.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:49:34

Label at a glance#

ProductPURELL Advanced Hand Sanitizer Foam
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN6
616805ethanol 0.7 ML/ML Topical FoamSCD6
616805ethanol 70 % Topical FoamSY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-030-17PURELL Advanced Hand Sanitizer Foam515 mL in 1 PACKAGELIQUID5156
21749-030-53PURELL Advanced Hand Sanitizer Foam535 mL in 1 PACKAGELIQUID5356
21749-030-89PURELL Advanced Hand Sanitizer Foam1200 mL in 1 PACKAGELIQUID12006
21749-030-97PURELL Advanced Hand Sanitizer Foam700 mL in 1 PACKAGELIQUID7006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-030PURELL ADVANCED HAND SANITIZER FOAM (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]64 package rows20250101_189bae12-9e19-454a-9789-d7308e8ffc29.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
21749-03021749-030-89, 21749-030-97, 21749-030-53, 21749-030-17

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 · 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
2a971bd7-cd93-e1e5-e063-6294a90a068f189bae12-9e19-454a-9789-d7308e8ffc292024-12-31Exact identifier
spl id: 2a971bd7-cd93-e1e5-e063-6294a90a068f
spl set id: 189bae12-9e19-454a-9789-d7308e8ffc29

Reported adverse events (FAERS/openFDA)#

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