Foot Powder
- Product NDC
- 0363-7999
- 11-digit product format
- 003637999
- Labeler code
- 0363
- Product ID
- 0363-7999_49786c9d-1a64-2c80-e063-6394a90a7150
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Walgreens Company
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-12
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Foot Powder
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 20 mg/g |
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 |
|---|
| 0363-7999-01 | Foot Powder | 71 g in 1 BOTTLE, PLASTIC | POWDER | 71 | | 5 |
| 0363-7999-03 | Foot Powder | 85 g in 1 BOTTLE, PLASTIC | POWDER | 85 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-7999 | FOOT POWDER (MICONAZOLE NITRATE) POWDER [WALGREENS COMPANY] | 2 | Current NDC, 2 package rows | 20241215_137a493b-6ed5-d649-e063-6294a90ac442.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-7999-01 | 00363799901 | 71 g in 1 BOTTLE, PLASTIC (0363-7999-01) | 71 g | 2024-03-12 | No | No | Historical |
| 0363-7999-03 | 00363799903 | 85 g in 1 BOTTLE, PLASTIC (0363-7999-03) | 85 g | 2025-12-17 | No | No | Historical |