Cutter Brand Hand Sanitizer

Product NDC
79364-1682
11-digit product format
793641682
Labeler code
79364
Product ID
79364-1682_ba706b46-033e-4378-8a9f-dd51308aff1a
Type
HUMAN OTC DRUG
Nonproprietary name
alcohol
Dosage form
AEROSOL
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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9be3ebe6-89e5-4e2f-8781-a389e7eb49e7Product name120250129
f76fb619-09b6-d149-3287-3661f7bc38cdProduct name320250124
62a0eedf-9497-47af-bccf-d51b8b15b067Product name120180307

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79364-1682-22024-01-30C16284748780-11030e365-5e6e-111a-e063-dadaa90a10e2Cutter ™ Brand Hand Sanitizer
79364-1682-52024-01-30C16284748780-11030e365-5e6e-111a-e063-dadaa90a10e2Cutter ™ Brand Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79364-1682-2Cutter Brand Hand Sanitizer70 g in 1 CANAEROSOL701
79364-1682-5Cutter Brand Hand Sanitizer141 g in 1 CANAEROSOL1411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79364-1682CUTTER BRAND HAND SANITIZER (ALCOHOL) AEROSOL [UNITED INDUSTRIES CORPORATION]1Legacy NDC, 2 package rows20201101_3a9f6446-ab38-466f-82b7-6452fa09b84b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
79364-1682-27936416820270 g in 1 CAN (79364-1682-2) 70 g2020-11-010000-00-00NoNoCurrent
79364-1682-579364168205141 g in 1 CAN (79364-1682-5) 141 g2020-11-010000-00-00NoNoCurrent