Lacura Extreme Blast

Product NDC
10889-110
11-digit product format
108890110
Labeler code
10889
Product ID
10889-110_e3832b92-a779-488b-97b3-7c23be1d2e4b
Type
HUMAN OTC DRUG
Nonproprietary name
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Dosage form
STICK
Route
CUTANEOUS
Labeler
VVF Kansas Services LLC
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-12-13
Marketing end
0000-00-00
Substance
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Active strength
250 mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10889-110-172019-10-29C16284748780-1960f7f55-d27d-8e05-e053-dbdaa90a074aLacura Extreme Blast (Aluminun Zirconium Trichlorohydrex Gly)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10889-110-17Lacura Extreme Blastanti-perspirant deodorant76 g in 1 PACKAGESTICK761

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10889-110LACURA EXTREME BLAST ANTI-PERSPIRANT DEODORANT (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) STICK [VVF KANSAS SERVICES LLC]1Legacy NDC, 1 package rows20101213_f2994b8a-1c60-43bb-b19e-1c7467624a50.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
10889-110-171088901101776 g in 1 PACKAGE76 gHistorical