PURELL Antiseptic Hand Gel

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 00:50:07

Label at a glance#

ProductPURELL Antiseptic Hand 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 GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21749-672-02PURELL Antiseptic Hand Gel60 mL in 1 PACKAGEGEL603
21749-672-12PURELL Antiseptic Hand Gel350 mL in 1 PACKAGEGEL3503
21749-672-16PURELL Antiseptic Hand Gel450 mL in 1 PACKAGEGEL4503
21749-672-89PURELL Antiseptic Hand Gel1200 mL in 1 PACKAGEGEL12003
21749-672-90PURELL Antiseptic Hand Gel1250 mL in 1 PACKAGEGEL12503
21749-672-97PURELL Antiseptic Hand Gel700 mL in 1 PACKAGEGEL7003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-672PURELL ANTISEPTIC HAND GEL (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]36 package rows20250101_b81452e9-b761-48ce-9eeb-1818bc64cc19.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21749-67221749-672-02, 21749-672-12, 21749-672-16, 21749-672-97, 21749-672-89, 21749-672-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
2a9687f5-a04e-ea3f-e063-6294a90a9db3b81452e9-b761-48ce-9eeb-1818bc64cc192024-12-31Exact identifier
spl id: 2a9687f5-a04e-ea3f-e063-6294a90a9db3
spl set id: b81452e9-b761-48ce-9eeb-1818bc64cc19

Reported adverse events (FAERS/openFDA)#

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