ProCure Antifungal
- Product NDC
- 55681-043
- 11-digit product format
- 556810043
- Labeler code
- 55681
- Product ID
- 55681-043_3d375325-ddae-f1e1-e063-6394a90a679f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate 2%
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Twin Med LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 g/100g
- 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
- ProCure Antifungal
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 2 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998461 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55681-043-03 | ProCure Antifungal | 85 g in 1 BOTTLE | POWDER | 85 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-043-03 | 55681004303 | 85 g in 1 BOTTLE (55681-043-03) | 85 g | 2025-12-01 | No | No | Current |