NDC 0065-0616-35 - Maxidex

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: 0065-0616
Requested NDC: 0065-0616-35
Package NDCs from labels: 0065-0616-35
Manufacturer: Alcon
Effective date: 2006-12-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Maxidex - Alcon	Alcon	2006-12-26	Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0065-0616-35	Maxidex	3.5 g in 1 TUBE	OINTMENT	3.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0065-0616	MAXIDEX (DEXAMETHASONE SODIUM PHOSPHATE) OINTMENT [ALCON]	1	1 package rows	20080313_863fb43c-dd33-485b-9385-744db7a98b83.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
dexamethasone sodium phosphate	ACTIVE INGREDIENT	AI9376Y64P	MAXIDEX (DEXAMETHASONE SODIUM PHOSPHATE) OINTMENT [ALCON]	1
dexamethasone phosphate	ACTIVE MOIETY	2BP70L44PR	MAXIDEX (DEXAMETHASONE SODIUM PHOSPHATE) OINTMENT [ALCON]	1
mineral oil	INACTIVE INGREDIENT		MAXIDEX (DEXAMETHASONE SODIUM PHOSPHATE) OINTMENT [ALCON]	1
white petrolatum	INACTIVE INGREDIENT	4T6H12BN9U	MAXIDEX (DEXAMETHASONE SODIUM PHOSPHATE) OINTMENT [ALCON]	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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6E79C53E-5BB9-31F8-DE1A-81B0BA2FD270			863fb43c-dd33-485b-9385-744db7a98b83	2006-12-26	Warnings, Adverse reactions	Exact identifier spl id: 6E79C53E-5BB9-31F8-DE1A-81B0BA2FD270 spl set id: 863fb43c-dd33-485b-9385-744db7a98b83

Reported adverse events (FAERS/openFDA)#

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