CANTHARIDIN 0.7%

Product NDC: 72934-9035
11-digit product format: 729349035
Labeler code: 72934
Product ID: 72934-9035_891ae88b-bacd-137f-e053-2a95a90a8f7d
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: CANTHARIDIN 0.7%
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: CANTHARIDIN
Active strength: 1 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 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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Status
72934-9035-9	72934903509	15 g in 1 VIAL	15 g	Historical