NDC 67402-050 - Desonate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 67402-050
Package NDCs from labels: 67402-050-60, 67402-050-03
Manufacturer: SkinMedica
Effective date: 2007-03-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Desonate - SkinMedica	SkinMedica	2007-03-30	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67402-050-03	Desonate	3.5 g in 5 TUBE	GEL	3.5		1
67402-050-60	Desonate	60 g in 1 TUBE	GEL	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67402-050	DESONATE (DESONIDE) GEL [SKINMEDICA]	1	2 package rows	20070517_A15D0DF0-3BCA-4FBC-A1D6-34A88C9A9665.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
desonide	ACTIVE INGREDIENT	J280872D1O	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
desonide	ACTIVE MOIETY	J280872D1O	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Carbopol 981	INACTIVE INGREDIENT		DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Edetate Disodium Dihydrate	INACTIVE INGREDIENT	7FLD91C86K	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Methylparaben	INACTIVE INGREDIENT		DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Propylene Glycol	INACTIVE INGREDIENT	6DC9Q167V3	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	DESONATE (DESONIDE) GEL [SKINMEDICA]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	DESONATE (DESONIDE) GEL [SKINMEDICA]	1

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DESONIDE	DESONIDE	Cintex Services, LLC	a6192416-09b4-47fa-e053-2a95a90add96	2020-07-31	Warnings, Adverse reactions	Exact identifier rxcui: 669081
F1E51B0A-E679-3706-A86F-444F00C22BCD			A15D0DF0-3BCA-4FBC-A1D6-34A88C9A9665	2007-03-30	Adverse reactions	Exact identifier spl id: F1E51B0A-E679-3706-A86F-444F00C22BCD spl set id: A15D0DF0-3BCA-4FBC-A1D6-34A88C9A9665

Reported adverse events (FAERS/openFDA)#

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