Fungus Master
- Product NDC
- 63742-098
- 11-digit product format
- 637420098
- Labeler code
- 63742
- Product ID
- 63742-098_36eb334e-246c-249f-e063-6294a90ab811
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MICONAZOLE NITRATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Clinical Resolution Laboratory, Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-06
- Substance
- MICONAZOLE NITRATE
- Active strength
- 20 mg/g
- 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
- Fungus Master
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998521 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63742-098-01 | Fungus Master | 30 g in 1 BOTTLE, GLASS | LOTION | 30 | | 1 |
| 63742-098-02 | Fungus Master | 59 g in 1 BOTTLE, GLASS | LOTION | 59 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63742-098-01 | 63742009801 | 30 g in 1 BOTTLE, GLASS (63742-098-01) | 30 g | 2025-06-06 | No | No | Historical |
| 63742-098-02 | 63742009802 | 59 g in 1 BOTTLE, GLASS (63742-098-02) | 59 g | 2025-06-06 | No | No | Historical |