PURELL Advanced Hand Sanitizer Refreshing Aloe Gel

Manufacturer
GOJO Industries, LLC
Effective date
2026-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:57:54

Label at a glance#

ProductPURELL Advanced Hand Sanitizer Refreshing Aloe Gel
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
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-735-02PURELL Advanced Hand Sanitizer Refreshing Aloe Gel60 mL in 1 BOTTLEGEL601
21749-735-08PURELL Advanced Hand Sanitizer Refreshing Aloe Gel236 mL in 1 BOTTLEGEL2361
21749-735-10PURELL Advanced Hand Sanitizer Refreshing Aloe Gel295 mL in 1 BOTTLEGEL2951
21749-735-20PURELL Advanced Hand Sanitizer Refreshing Aloe Gel591 mL in 1 BOTTLEGEL5911

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-73521749-735-02, 21749-735-08, 21749-735-10, 21749-735-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
521c318f-ecf2-6499-e063-6294a90a2316521c3139-1b75-1f17-e063-6394a90a9da22026-05-18Exact identifier
spl id: 521c318f-ecf2-6499-e063-6294a90a2316
spl set id: 521c3139-1b75-1f17-e063-6394a90a9da2

Reported adverse events (FAERS/openFDA)#

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