Lotrimin
- Product NDC
- 11523-0150
- 11-digit product format
- 115230150
- Labeler code
- 11523
- Product ID
- 11523-0150_48850e7a-a19c-ce92-e063-6394a90afaaf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole nitrate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Bayer HealthCare LLC.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-06
- 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
- Lotrimin
- Brand name suffix
- AF Jock Itch
- 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 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11523-0150-1 | LotriminAF Jock Itch | 177 g in 1 CAN | POWDER | 177 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11523-0150 | LOTRIMIN AF JOCK ITCH (MICONAZOLE NITRATE) POWDER [BAYER HEALTHCARE LLC.] | 1 | Current NDC, 1 package rows | 20240329_1300d84f-d7ff-ec57-e063-6294a90ae0de.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 |
|---|
| 11523-0150-1 | 11523015001 | 177 g in 1 CAN (11523-0150-1) | 177 g | 2023-11-06 | No | No | Historical |