CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%- cantharidin 1% / podophyllum resin 5% / salicylic acid 30% liquid
Sincerus Florida, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

asd

NDC 72934- 9036-9 CANTHARIDIN 1% / PODOPHYLLUM RESIN USP 5% / SALICYLIC ACID USP 30%. Liquid 15 gm

sdf

CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%
cantharidin 1% / podophyllum resin 5% / salicylic acid 30% liquid

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:72934-9036
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	30 g in 100 g
CANTHARIDIN (UNII: IGL471WQ8P) (CANTHARIDIN - UNII:IGL471WQ8P)	CANTHARIDIN	1 g in 100 g
PODOPHYLLUM RESIN (UNII: 16902YVY2B) (PODOPHYLLUM RESIN - UNII:16902YVY2B)	PODOPHYLLUM RESIN	5 g in 100 g

Product Characteristics
Color	brown (traslucent)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-9036-9	15 g in 1 VIAL; Type 0: Not a Combination Product	05/17/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		05/17/2019

Labeler - Sincerus Florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-9036)