NDC 11695-2201 - Micazole
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
- 11695-2201
- Package NDCs from labels
- 11695-2201-6, 11695-2201-1, 11695-2201-2
- Manufacturer
- Butler Animal health Supply, LLC dba Covetrus North America | FIRST PRIORITY INCORPORATED
- Effective date
- 2019-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Micazole Lotion ™ 1% & Micazole Spray ™ 1% | Butler Animal health Supply, LLC dba Covetrus North America | FIRST PRIORITY INCORPORATED | 2019-08-20 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MICONAZOLE NITRATE | ACTIVE INGREDIENT | VW4H1CYW1K | MICAZOLE (MICAONAZOLE) SPRAY [BUTLER SCHEIN ANIMAL HEALTH] | 1 | |
| MICONAZOLE | ACTIVE MOIETY | 7NNO0D7S5M | MICAZOLE (MICAONAZOLE) SPRAY [BUTLER SCHEIN ANIMAL HEALTH] | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.