NDC 0062-5437 - MONISTAT 3
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
- 0062-5437
- Package NDCs from labels
- 0062-5437-01
- Manufacturer
- ORTHO PHARMACEUTICAL CORPORATION
- Effective date
- 2006-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MONISTAT 3 - ORTHO PHARMACEUTICAL CORPORATION | ORTHO PHARMACEUTICAL CORPORATION | 2006-12-31 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0062-5437-01 | MONISTAT 3 | 3 in 1 PACKAGE | SUPPOSITORY | 3 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| miconazole nitrate | ACTIVE INGREDIENT | VW4H1CYW1K | MONISTAT 3 (MICONAZOLE NITRATE) SUPPOSITORY [ORTHO PHARMACEUTICAL CORPORATION] | 1 | |
| miconazole | ACTIVE MOIETY | 7NNO0D7S5M | MONISTAT 3 (MICONAZOLE NITRATE) SUPPOSITORY [ORTHO PHARMACEUTICAL CORPORATION] | 1 | |
| hydrogenated vegetable oil | INACTIVE INGREDIENT | MONISTAT 3 (MICONAZOLE NITRATE) SUPPOSITORY [ORTHO PHARMACEUTICAL CORPORATION] | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Signature Care Miconazole 3 | MICONAZOLE NITRATE | Safeway | 191e448b-0410-4102-82ae-a3387b27b227 | 2021-02-04 | Warnings | 992765 |
| Miconazole Nitrate | MICONAZOLE NITRATE | Actavis Pharma, Inc. | aa9e250b-f317-42cb-b8d2-e85de56f4ef7 | 2020-10-21 | Adverse reactions | 992765 |
| A1CD682A-FA73-491D-B276-8C96D801B083 | A1CD682A-FA73-491D-B276-8C96D801B083 | 2006-12-31 | Adverse reactions | A1CD682A-FA73-491D-B276-8C96D801B083 A1CD682A-FA73-491D-B276-8C96D801B083 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.