PURELL Advanced E3 Rated Instant Hand Sanitizer Foam

Product NDC
21749-802
Requested package NDC
21749-802-51
11-digit product format
217490802
Labeler code
21749
Product ID
21749-802_2916dce7-fee4-552c-e063-6294a90a5cb5
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
GOJO Industries, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-06-01
Substance
ALCOHOL
Active strength
.7 mL/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage21749-80221749-802-51DDiscontinued by firm2026-08-11

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…

Additional Listing Data#

Finished product
Yes
Brand name base
PURELL Advanced E3 Rated Instant Hand Sanitizer Foam
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALCOHOL.7 mL/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3K9958V90MInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
616805Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1f78370b-132a-4759-8cbc-b5e093f90f8dAvailable on FDA.report

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
21749-802-51PURELL Advanced E3 Rated Instant Hand Sanitizer Foam550 mL in 1 BOTTLELIQUID5504
21749-802-53PURELL Advanced E3 Rated Instant Hand Sanitizer Foam535 mL in 1 BOTTLELIQUID5354
21749-802-89PURELL Advanced E3 Rated Instant Hand Sanitizer Foam1200 mL in 1 BOTTLELIQUID12004
21749-802-97PURELL Advanced E3 Rated Instant Hand Sanitizer Foam700 mL in 1 BOTTLELIQUID7004

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-802PURELL ADVANCED E3 RATED INSTANT HAND SANITIZER FOAM (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]4Current NDC, Legacy NDC, 4 package rows20241215_1f78370b-132a-4759-8cbc-b5e093f90f8d.zip

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
PURELL Advanced E3 Rated Instant Hand Sanitizer FoamALCOHOLGOJO Industries, Inc.1f78370b-132a-4759-8cbc-b5e093f90f8d2024-12-12WarningsExact identifier
ndc (package): 21749-802-51
ndc (product): 21749-802
ndc11 (package): 21749080251

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616805ethanol 70 % Topical FoamPSN1f78370b-132a-4759-8cbc-b5e093f90f8d4
616805ethanol 0.7 ML/ML Topical FoamSCD1f78370b-132a-4759-8cbc-b5e093f90f8d4
616805ethanol 70 % Topical FoamSY1f78370b-132a-4759-8cbc-b5e093f90f8d4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-802-5121749080251550 mL in 1 BOTTLE (21749-802-51) 550 ml2012-06-010000-00-00NoNoCurrent