NDC 11523-0010-01 - Lotrimin Daily Prevention Deo
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 11523-0010
- Requested NDC
- 11523-0010-01
- Package NDCs from labels
- 11523-0010-1, 11523-0010-2, 11523-0010-01
- Manufacturer
- Bayer HealthCare LLC.
- Effective date
- 2025-12-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lotrimin Daily Prevention Deo Powder Spray UI 1612507 | Bayer HealthCare LLC. | 2025-12-04 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11523-0010-1 | Lotrimin Daily Prevention Deo | 160 g in 1 CAN | AEROSOL, POWDER | 160 | 10 | |
| 11523-0010-2 | Lotrimin Daily Prevention Deo | 133 g in 1 CAN | AEROSOL, POWDER | 133 | 10 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11523-0010 | LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE) AEROSOL, POWDER [BAYER HEALTHCARE LLC.] | 9 | Current NDC, Legacy NDC, 2 package rows | 20241208_9e8bfb78-ad81-93d0-e053-2995a90aa41d.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.