FDA.reportPublic FDA data

PURELL Advanced Hand Sanitizer be Vibrant

Product NDC
21749-028
Requested package NDC
21749-028-08
11-digit product format
217490028
Labeler code
21749
Product ID
21749-028_48366d7a-55a5-901e-e063-6294a90a677d
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
GEL
Route
TOPICAL
Labeler
GOJO Industries, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-12-22
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 packagepackage21749-02821749-028-08DDiscontinued by firm2026-09-14

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
PURELL Advanced Hand Sanitizer be Vibrant
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
581662Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
3a991a7f-1289-4aeb-82f9-8cebd6a389b5Available 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
21749-028-01PURELL Advanced Hand Sanitizer be Vibrant30 mL in 1 PACKAGEGEL304
21749-028-02PURELL Advanced Hand Sanitizer be Vibrant59 mL in 1 PACKAGEGEL594
21749-028-04PURELL Advanced Hand Sanitizer be Vibrant118 mL in 1 PACKAGEGEL1184
21749-028-08PURELL Advanced Hand Sanitizer be Vibrant236 mL in 1 PACKAGEGEL2364
21749-028-10PURELL Advanced Hand Sanitizer be Vibrant295 mL in 1 PACKAGEGEL2954
21749-028-12PURELL Advanced Hand Sanitizer be Vibrant354 mL in 1 PACKAGEGEL3544
21749-028-16PURELL Advanced Hand Sanitizer be Vibrant473 mL in 1 PACKAGEGEL4734
21749-028-20PURELL Advanced Hand Sanitizer be Vibrant591 mL in 1 PACKAGEGEL5914
21749-028-45PURELL Advanced Hand Sanitizer be Vibrant450 mL in 1 PACKAGEGEL4504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21749-028PURELL ADVANCED HAND SANITIZER BE VIBRANT (ALCOHOL) GEL [GOJO INDUSTRIES, INC.]3Current NDC, Legacy NDC, 9 package rows20241208_3a991a7f-1289-4aeb-82f9-8cebd6a389b5.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 Hand Sanitizer be VibrantALCOHOLGOJO Industries, Inc.3a991a7f-1289-4aeb-82f9-8cebd6a389b52026-01-12WarningsExact identifier
ndc (package): 21749-028-08
ndc (product): 21749-028
ndc11 (package): 21749002808

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
581662ethanol 70 % Topical GelPSN3a991a7f-1289-4aeb-82f9-8cebd6a389b54
581662ethanol 0.7 ML/ML Topical GelSCD3a991a7f-1289-4aeb-82f9-8cebd6a389b54
581662ethanol 70 % Topical GelSY3a991a7f-1289-4aeb-82f9-8cebd6a389b54
581662ethyl alcohol 70 % Topical GelSY3a991a7f-1289-4aeb-82f9-8cebd6a389b54

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21749-028-0821749002808236 mL in 1 PACKAGE (21749-028-08) 236 ml2016-12-220000-00-00NoNoCurrent