Warrior Antifungal Foot
- Product NDC
- 72839-961
- 11-digit product format
- 728390961
- Labeler code
- 72839
- Product ID
- 72839-961_29b73d29-5847-610c-e063-6394a90aca16
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate 2%
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Derma Care Research Labs, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-02-02
- 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
- Warrior Antifungal Foot
- 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 |
|---|
| 72839-961-02 | Warrior Antifungal Foot | 71 g in 1 BOTTLE | POWDER | 71 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72839-961 | WARRIOR ANTIFUNGAL FOOT (MICONAZOLE NITRATE 2%) POWDER [DERMA CARE RESEARCH LABS, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241222_cf2e9dc1-275b-4454-e053-2995a90af295.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 |
|---|
| 72839-961-02 | 72839096102 | 71 g in 1 BOTTLE (72839-961-02) | 71 g | 2021-02-02 | 0000-00-00 | No | No | Current |