Antifungal Body
- Product NDC
- 68599-0206
- 11-digit product format
- 685990206
- Labeler code
- 68599
- Product ID
- 68599-0206_1acb3889-ffea-8cd2-e063-6394a90a3ecb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- McKesson
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-06-01
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 mg/100mL
- 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
- Antifungal Body
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 2 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998483 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68599-0206-4 | Antifungal Body | 118 mL in 1 TUBE | CREAM | 118 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68599-0206 | ANTIFUNGAL BODY (MICONAZOLE NITRATE) CREAM [MCKESSON] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240616_4fb9aece-0baa-475e-e054-00144ff8d46c.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 |
|---|
| 68599-0206-4 | 68599020604 | 118 mL in 1 TUBE (68599-0206-4) | 118 ml | 2017-06-01 | 0000-00-00 | No | No | Current |