Fusion Antibacterial Wipes

Product NDC
80336-004
11-digit product format
803360004
Labeler code
80336
Product ID
80336-004_c5f2f7cc-662a-2a4d-e053-2995a90ad87c
Type
HUMAN OTC DRUG
Nonproprietary name
Antibacterial Wet Wipes
Dosage form
CLOTH
Route
TOPICAL
Labeler
Fusion Products Ltd.
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2020-10-23
Marketing end
0000-00-00
Substance
BENZALKONIUM CHLORIDE
Active strength
0 1/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80336-004-092023-01-30C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes
80336-004-092022-08-23C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes
80336-004-092022-07-29C16284748780-1e4f33bdf-aa55-d8a0-e053-dadaa90a6e4eFusion Antibacterial Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80336-004-09Fusion Antibacterial Wipes70 in 1 BOTTLECLOTH704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80336-004FUSION ANTIBACTERIAL WIPES (ANTIBACTERIAL WET WIPES) CLOTH [FUSION PRODUCTS LTD.]4Legacy NDC, 1 package rows20210630_b2c53fa7-a74f-8fc1-e053-2a95a90a8942.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80336-004-098033600040970 CLOTH in 1 BOTTLE (80336-004-09) 70 cloth2020-10-230000-00-00NoNoCurrent