Miconazole Nitrate
- Product NDC
- 56104-907
- 11-digit product format
- 561040907
- Labeler code
- 56104
- Product ID
- 56104-907_42f401f0-e0c2-bad0-e063-6294a90ad799
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antifungal Powder Spray
- Dosage form
- AEROSOL, POWDER
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-27
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Miconazole Nitrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998428 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-907-01 | Miconazole Nitrate | 130 g in 1 CAN | AEROSOL, POWDER | 130 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 56104-907-01 | 56104090701 | 130 g in 1 CAN (56104-907-01) | 130 g | 2025-06-27 | No | No | Current |