NDC 13985-438 - VetraSeb CeraDerm P

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: 13985-438
Package NDCs from labels: 13985-438-08, 13985-438-16
Manufacturer: MWI/VETONE | Ceva Sante Animale
Effective date: 2021-04-06
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
VetraSeb CeraDerm P - MWI/VETONE \| Ceva Sante Animale	MWI/VETONE \| Ceva Sante Animale	2021-04-06	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
13985-438-08	VetraSeb CeraDermP	237 mL in 1 BOTTLE, PLASTIC	SHAMPOO	237		1
13985-438-16	VetraSeb CeraDermP	473 mL in 1 BOTTLE, PLASTIC	SHAMPOO	473		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
13985-438	VETRASEB CERADERM P (PRAMOXINE HYDROCHLORIDE) SHAMPOO [MWI/VETONE]	1	2 package rows	20210407_fca6ae64-67c9-41d8-8747-15f741dec916.zip

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 77 of 77 · 1,522 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: TU7HW0W0QT unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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