NDC 54108-8712-01 - Derma E Eczema Relief
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
- 54108-8712
- Requested NDC
- 54108-8712-01
- Package NDCs from labels
- 54108-8712-1, 54108-8712-01
- Manufacturer
- derma e | Topiderm, Inc.
- Effective date
- 2024-06-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Derma E Eczema Relief | derma e | Topiderm, Inc. | 2024-06-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54108-8712-1 | Derma E Eczema Relief | 175 mL in 1 TUBE | LOTION | 175 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 54108-8712 | DERMA E ECZEMA RELIEF (OATMEAL) LOTION [DERMA E] | 1 | Current NDC, 1 package rows | 20240625_767c4a76-8ccb-4530-9b4b-a7ea1a596c7f.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.