NDC 46783-803 - Mederma PM
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
- 46783-803
- Package NDCs from labels
- 46783-803-30
- Manufacturer
- Merz North America
- Effective date
- 2024-03-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Mederma PM - Merz North America | Merz North America | 2024-03-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 46783-803-30 | Mederma PM | 1 in 1 BOX | CREAM | 1 | 1 | |
| 46783-803-30 | Mederma PM | 30 mL in 1 TUBE | CREAM | 30 | 1 |
DailyMed Dashboard NDC Coverage#
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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| L-Leucine High 7414 | L-LEUCINE HIGH | Professional Complementary Health Formulas | 261acb1f-4767-4ac9-92ba-8f3f60b57b92 | 2026-01-08 | Warnings | GMW67QNF9C |
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| Dehydrated Alcohol | ALCOHOL | BPI Labs, LLC | 314b1dab-8f4f-49ae-a105-f974842818b8 | 2026-01-05 | Warnings, Adverse reactions | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.