CANTHARIDIN 0.7%

Manufacturer: Sincerus Florida, LLC
Effective date: 2019-05-17
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:28:50

Label at a glance#

ProductCANTHARIDIN 0.7%

Active ingredientCANTHARIDIN

Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

sdgf

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

Active, inactive

COMPONENTS

azsd

NDC 72934- 9035-9 CANTHARIDIN 0.7%. Liquid 15 gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
9cb53635-25f5-4f32-92e9-047a63fb4e56	Product name	1	20231023

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72934-9035-9	2021-01-29	C162847	48780-1	ba0f9c33-4530-a910-e053-dadaa90a0b85	CANTHARIDIN 0.7%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72934-9035-9	CANTHARIDIN 0.7%	15 g in 1 VIAL	LIQUID	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72934-9035	CANTHARIDIN 0.7% LIQUID [SINCERUS FLORIDA, LLC]	1	Legacy NDC, 1 package rows	20190518_891ae88b-bacc-137f-e053-2a95a90a8f7d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

CANTHARIDIN 0.7%
CANTHARIDIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72934-9035	72934-9035-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CANTHARIDIN	IGL471WQ8P	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
891ae88b-bacd-137f-e053-2a95a90a8f7d			891ae88b-bacc-137f-e053-2a95a90a8f7d	2019-05-17	Adverse reactions	Exact identifier spl id: 891ae88b-bacd-137f-e053-2a95a90a8f7d spl set id: 891ae88b-bacc-137f-e053-2a95a90a8f7d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.