Miconazole Nitrate
- Product NDC
- 56104-121
- 11-digit product format
- 561040121
- Labeler code
- 56104
- Product ID
- 56104-121_29b6fb49-f5fd-d406-e063-6294a90ace19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antifungal Miconazole Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-12
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2.6 g/130g
- 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 | 2.6 g/130g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998428 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-121-01 | Miconazole Nitrate | 130 g in 1 CANISTER | AEROSOL, SPRAY | 130 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-121 | MICONAZOLE NITRATE (ANTIFUNGAL MICONAZOLE POWDER SPRAY) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250227_dc7a23bb-b246-89b1-e053-2995a90a9f2d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-121-01 | 56104012101 | 130 g in 1 CANISTER (56104-121-01) | 130 g | 2022-04-12 | 0000-00-00 | No | No | Current |