Assured

Product NDC
33992-0828
11-digit product format
339920828
Labeler code
33992
Product ID
33992-0828_6d3d1a6e-8a58-437d-b7a7-2d1b486a141c
Type
HUMAN OTC DRUG
Nonproprietary name
ALUMINUM SULFATE
Dosage form
POWDER
Route
TOPICAL
Labeler
Greenbrier International
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-04-20
Marketing end
0000-00-00
Substance
ALUMINUM SULFATE
Active strength
56 g/100g
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
33992-0828-12020-01-31C16284748780-19d75b9d0-a3d2-f424-e053-dadaa90a57cead067b04-ff57-44ab-a6cb-f524f8294989

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33992-0828-1Assured28 g in 1 BLISTER PACKPOWDER282

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33992-0828ASSURED (ALUMINUM SULFATE) POWDER [GREENBRIER INTERNATIONAL]2Legacy NDC, 1 package rows20160425_ad067b04-ff57-44ab-a6cb-f524f8294989.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
33992-0828-13399208280128 g in 1 BLISTER PACK28 gHistorical