PURELL Advanced Instant Hand Sanitizer

Product NDC
21749-807
Requested package NDC
21749-807-53
11-digit product format
217490807
Labeler code
21749
Product ID
21749-807_48375f35-5b61-d2fe-e063-6294a90a558a
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
2011-04-11
Substance
ALCOHOL
Active strength
.7 mL/mL
NDC exclude flag
No
Listing certified through
2027-12-31
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 packagepackage21749-80721749-807-53DDiscontinued by firm2026-08-11

Additional Listing Data#

Finished product
Yes
Brand name base
PURELL Advanced Instant Hand Sanitizer
Listing expiration
2027-12-31

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
3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e5Available 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
21749-807-17PURELL Advanced Instant Hand Sanitizer515 mL in 1 BOTTLE, PUMPLIQUID51511
21749-807-22PURELL Advanced Instant Hand Sanitizer200 mL in 1 BOTTLE, PUMPLIQUID20011
21749-807-23PURELL Advanced Instant Hand Sanitizer222 mL in 1 BOTTLE, PUMPLIQUID22211
21749-807-30PURELL Advanced Instant Hand Sanitizer300 mL in 1 PACKAGELIQUID30011
21749-807-31PURELL Advanced Instant Hand Sanitizer45 mL in 1 BOTTLE, PUMPLIQUID4511
21749-807-33PURELL Advanced Instant Hand Sanitizer1000 mL in 1 BOTTLE, PUMPLIQUID100011
21749-807-50PURELL Advanced Instant Hand Sanitizer189271 mL in 1 PACKAGELIQUID18927111
21749-807-51PURELL Advanced Instant Hand Sanitizer550 mL in 1 BOTTLE, PUMPLIQUID55011
21749-807-53PURELL Advanced Instant Hand Sanitizer535 mL in 1 BOTTLE, PUMPLIQUID53511
21749-807-80PURELL Advanced Instant Hand Sanitizer800 mL in 1 PACKAGELIQUID80011
21749-807-89PURELL Advanced Instant Hand Sanitizer1200 mL in 1 BOTTLE, PUMPLIQUID120011
21749-807-97PURELL Advanced Instant Hand Sanitizer700 mL in 1 PACKAGELIQUID70011

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-807PURELL ADVANCED INSTANT HAND SANITIZER (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.]10Current NDC, Legacy NDC, 12 package rows20241215_3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e5.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 Instant Hand SanitizerALCOHOLGOJO Industries, Inc.3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e52026-01-12WarningsExact identifier
ndc (package): 21749-807-53
ndc (product): 21749-807
ndc11 (package): 21749080753

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
616805ethanol 70 % Topical FoamPSN3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e511
616805ethanol 0.7 ML/ML Topical FoamSCD3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e511
616805ethanol 70 % Topical FoamSY3c3b14e1-4a9d-4ebb-b6b6-ab0173ac06e511

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-807-5321749080753535 mL in 1 BOTTLE, PUMP (21749-807-53) 535 ml2011-04-110000-00-00NoNoCurrent