FDA.reportPublic FDA data

CYZONE XPRESS YOUR BODY CLARITY

Product NDC
13537-989
11-digit product format
135370989
Labeler code
13537
Product ID
13537-989_31e7036c-7e8a-4562-b2eb-b3999df271e5
Type
HUMAN OTC DRUG
Nonproprietary name
ALUMINUM SESQUICHLOROHYDRATE
Dosage form
EMULSION
Route
TOPICAL
Labeler
Ventura Corporation LTD
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2016-08-09
Marketing end
0000-00-00
Substance
ALUMINUM SESQUICHLOROHYDRATE
Active strength
0 g/mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13537-989-012025-11-05C16284748780-19d75b9d1-27ed-f424-e053-dadaa90a57ceCYZONE XPRESS YOUR BODY CLARITY
13537-989-012020-01-31C16284748780-19d75b9d1-27ed-f424-e053-dadaa90a57ceCYZONE XPRESS YOUR BODY CLARITY

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13537-989CYZONE XPRESS YOUR BODY CLARITY (ALUMINUM SESQUICHLOROHYDRATE) EMULSION [VENTURA CORPORATION LTD]1Legacy NDC20160809_eec3c556-3aff-44c4-b4ad-acf69ee81c79.zip