NDC 86067-0108 - Sur-Hoof

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: 86067-0108
Package NDCs from labels: 86067-0108-1, 86067-0108-2, 86067-0108-3
Manufacturer: Surpass Chemical. Company, Inc.
Effective date: 2024-05-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SUR-HOOF	Surpass Chemical. Company, Inc.	2024-05-10	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
86067-0108-1	Sur-Hoof	9.98 kg in 1 JUG	SOLUTION	9.98	2
86067-0108-2	Sur-Hoof	222.26 kg in 1 DRUM	SOLUTION	222.26	2
86067-0108-3	Sur-Hoof	1293.65 kg in 1 CONTAINER	SOLUTION	1293.65	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86067-0108	SUR-HOOF (FORMALDEHYDE) SOLUTION [SURPASS CHEMICAL. COMPANY, INC.]	2	3 package rows	20240511_83f98dd4-92a6-4a52-b5dd-4acd1ad3b114.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 18 of 18 · 341 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL

Reported adverse events (FAERS/openFDA)#

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