Cutter Brand Foaming Hand Sanitizer

Product NDC
79364-1681
11-digit product format
793641681
Labeler code
79364
Product ID
79364-1681_267af434-8d1a-4ac5-9941-33b3b96d1ecf
Type
HUMAN OTC DRUG
Nonproprietary name
Alcohol
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
United Industries Corporation
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-11-01
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
1 g/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79364-1681-32024-01-30C16284748780-11030e365-0910-111a-e063-dadaa90a10e2Cutter ™ Brand Foaming Hand Sanitizer
79364-1681-62024-01-30C16284748780-11030e365-0910-111a-e063-dadaa90a10e2Cutter ™ Brand Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79364-1681-3Cutter Brand Foaming Hand Sanitizer85 g in 1 CANAEROSOL, FOAM851
79364-1681-6Cutter Brand Foaming Hand Sanitizer198 g in 1 CANAEROSOL, FOAM1981

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79364-1681CUTTER BRAND FOAMING HAND SANITIZER (ALCOHOL) AEROSOL, FOAM [UNITED INDUSTRIES CORPORATION]1Legacy NDC, 2 package rows20201101_2cf13e09-d0de-4c7b-8d66-8165e89be36c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79364-1681-37936416810385 g in 1 CAN (79364-1681-3) 85 g2020-11-010000-00-00NoNoCurrent
79364-1681-679364168106198 g in 1 CAN (79364-1681-6) 198 g2020-11-010000-00-00NoNoCurrent