NDC 64892-018 - HB Copper CB

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: 64892-018
Package NDCs from labels: 64892-018-21, 64892-018-88
Manufacturer: Wausau Chemical
Effective date: 2019-12-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
HB Copper CB - Wausau Chemical	Wausau Chemical	2019-12-13	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64892-018-21	HB Copper CB	208.2 L in 1 DRUM	SOLUTION	208.2		1
64892-018-88	HB Copper CB	1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK	SOLUTION	1040		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64892-018	HB COPPER CB (COPPER FOOTBATH) SOLUTION [WAUSAU CHEMICAL]	1	2 package rows	20191218_f0da9758-c448-40a4-a84b-015345db4dad.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
COPPER	CUPRIC CHLORIDE	Hospira, Inc.	a84d61a4-8e7f-4be1-aba6-f633b334aafc	2026-05-18	Warnings, Adverse reactions	Name fallback brand name: COPPER

Reported adverse events (FAERS/openFDA)#

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