Zeasorb Athletes Foot
- Product NDC
- 0316-8000
- 11-digit product format
- 003168000
- Labeler code
- 0316
- Product ID
- 0316-8000_48340802-e215-04b8-e063-6394a90ad0fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MICONAZOLE NITRATE
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Crown Laboratories
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-19
- 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
- Zeasorb Athletes Foot
- 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, 1437793 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0316-8000-01 | Zeasorb Athletes Foot | 71 g in 1 BOTTLE, PLASTIC | POWDER | 71 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0316-8000 | ZEASORB ATHLETES FOOT (MICONAZOLE NITRATE) POWDER [CROWN LABORATORIES] | 1 | Current NDC, 1 package rows | 20231111_09bb313e-90cb-5629-e063-6294a90ac268.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 |
|---|
| 0316-8000-01 | 00316800001 | 71 g in 1 BOTTLE, PLASTIC (0316-8000-01) | 71 g | 2023-10-19 | No | No | Historical |