NDC 64892-024-88 - 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
- 64892-024-88
- 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 | Type |
|---|---|---|---|
| HB Zinc Supreme - Wausau Chemical | Wausau Chemical | 2020-01-07 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64892-024-16 | HB Zinc Supreme | 18.9 L in 1 PAIL | SOLUTION | 18.9 | 1 | |
| 64892-024-17 | HB Zinc Supreme | 56.78 L in 1 DRUM | SOLUTION | 56.78 | 1 | |
| 64892-024-18 | HB Zinc Supreme | 113.6 L in 1 DRUM | SOLUTION | 113.6 | 1 | |
| 64892-024-21 | HB Zinc Supreme | 208.2 L in 1 DRUM | SOLUTION | 208.2 | 1 | |
| 64892-024-88 | HB Zinc Supreme | 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK | SOLUTION | 1040 | 1 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.