Triple Antifungal
- Product NDC
- 16864-040
- 11-digit product format
- 168640040
- Labeler code
- 16864
- Product ID
- 16864-040_4d63f2a2-f113-d739-e063-6394a90a2d27
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Advantice Health, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-09-01
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 g/100g
- 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
- Triple Antifungal
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 2 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998442, 998460 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16864-040-02 | Triple Antifungal | 1 in 1 CARTON | OINTMENT | 1 | | 4 |
| 16864-040-02 | Triple Antifungal | 56.7 g in 1 TUBE | OINTMENT | 56.7 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16864-040 | TRIPLE ANTIFUNGAL (MICONAZOLE NITRATE) OINTMENT [ADVANTICE HEALTH, LLC] | 3 | Current NDC, Legacy NDC, 2 package rows | 20241215_9a47fb1b-a41f-4c8a-8e43-7332853c308e.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 |
|---|
| 16864-040-02 | 16864004002 | 1 TUBE in 1 CARTON (16864-040-02) / 56.7 g in 1 TUBE | 1 tube | 2021-09-01 | 0000-00-00 | No | No | Current |