FDA.reportPublic FDA data

NDC 64892-024-21 - HB Zinc Supreme

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
64892-024
Requested NDC
64892-024-21
Package NDCs from labels
64892-024-16, 64892-024-17, 64892-024-18, 64892-024-21, 64892-024-88
Manufacturer
Wausau Chemical
Effective date
2020-01-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
HB Zinc Supreme - Wausau ChemicalWausau Chemical2020-01-07OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64892-024-16HB Zinc Supreme18.9 L in 1 PAILSOLUTION18.91
64892-024-17HB Zinc Supreme56.78 L in 1 DRUMSOLUTION56.781
64892-024-18HB Zinc Supreme113.6 L in 1 DRUMSOLUTION113.61
64892-024-21HB Zinc Supreme208.2 L in 1 DRUMSOLUTION208.21
64892-024-88HB Zinc Supreme1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKSOLUTION10401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64892-024HB ZINC SUPREME (ZINC FOOTBATH) SOLUTION [WAUSAU CHEMICAL]15 package rows20200114_27b14c37-e2b0-45bb-a96e-fd1cc8b77e48.zip

Reported adverse events (FAERS/openFDA)#

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