CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%

Product NDC
72934-9036
11-digit product format
729349036
Labeler code
72934
Product ID
72934-9036_891a7037-9b8b-cbd3-e053-2a95a90a7006
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Sincerus Florida, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-05-17
Marketing end
0000-00-00
Substance
SALICYLIC ACID; CANTHARIDIN; PODOPHYLLUM RESIN
Active strength
30 g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9cb53635-25f5-4f32-92e9-047a63fb4e56Product name120231023

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-9036-92021-01-29C16284748780-1ba0f9c33-1cd3-a910-e053-dadaa90a0b85CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-9036-9CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%15 g in 1 VIALLIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-9036CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30% LIQUID [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190518_891a7037-9b8a-cbd3-e053-2a95a90a7006.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
72934-9036-97293490360915 g in 1 VIAL15 gHistorical