Miconazole Foot Powder
- Product NDC
- 42669-073
- 11-digit product format
- 426690073
- Labeler code
- 42669
- Product ID
- 42669-073_efbcd327-3ea4-6ce1-e053-2995a90ac843
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Davion, Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-08-19
- Marketing end
- 0000-00-00
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 g/100g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42669-073-01 | 42669007301 | 78 g in 1 BOTTLE, PLASTIC (42669-073-01) | 78 g | 2022-08-19 | 0000-00-00 | No | No | Current |