Anti-Fungal Powder
- Product NDC
- 30142-947
- 11-digit product format
- 301420947
- Labeler code
- 30142
- Product ID
- 30142-947_426575be-9907-72e8-e063-6294a90a7e33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- The Kroger Co.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-10-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VW4H1CYW1K | MICONAZOLE NITRATE | 22832-87-7 | MICONAZOLE NITRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 30142-947-71 | 30142094771 | 71 g in 1 BOTTLE, PLASTIC (30142-947-71) | 71 g | 2024-10-01 | No | No | Historical |