NDC 0071-3070 - Chloromycetin

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: 0071-3070
Package NDCs from labels: 0071-3070-07
Manufacturer: PARKE-DAVIS
Effective date: 2006-10-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Chloromycetin - PARKE-DAVIS	PARKE-DAVIS	2006-10-08	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0071-3070-07	Chloromycetin	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
0071-3070	CHLOROMYCETIN (CHLORAMPHENICOL) OINTMENT [PARKE-DAVIS]	1	1 package rows	20061117_698AAA0A-9FD3-40C2-EC93-0DC2170A75BA.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
chloramphenicol	ACTIVE INGREDIENT	66974FR9Q1	CHLOROMYCETIN (CHLORAMPHENICOL) OINTMENT [PARKE-DAVIS]	1
chloramphenicol	ACTIVE MOIETY	66974FR9Q1	CHLOROMYCETIN (CHLORAMPHENICOL) OINTMENT [PARKE-DAVIS]	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
698AAA0A-9FD3-40C2-EC93-0DC2170A75BA			698AAA0A-9FD3-40C2-EC93-0DC2170A75BA	2006-10-08	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: 698AAA0A-9FD3-40C2-EC93-0DC2170A75BA spl set id: 698AAA0A-9FD3-40C2-EC93-0DC2170A75BA

Reported adverse events (FAERS/openFDA)#

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