Lotrimin AF
- Product NDC
- 11523-0134
- 11-digit product format
- 115230134
- Labeler code
- 11523
- Product ID
- 11523-0134_4526e0ac-2219-182b-e063-6294a90a3a3b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole nitrate
- Dosage form
- AEROSOL, POWDER
- Route
- TOPICAL
- Labeler
- Bayer Healthcare LLC.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-26
- 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
- Lotrimin AF
- 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 | 998428 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11523-0134-1 | Lotrimin AF | 133 g in 1 CAN | AEROSOL, POWDER | 133 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11523-0134 | LOTRIMIN AF (MICONAZOLE NITRATE) AEROSOL, POWDER [BAYER HEALTHCARE LLC.] | 1 | Current NDC, 1 package rows | 20240524_163996c6-af54-21ac-e063-6394a90ac05c.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 |
|---|
| 11523-0134-1 | 11523013401 | 133 g in 1 CAN (11523-0134-1) | 133 g | 2024-02-26 | No | No | Historical |