NDC 79481-0043-01 - Meijer Medicated Foot Powder
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
- 79481-0043
- Requested NDC
- 79481-0043-01
- Package NDCs from labels
- 79481-0043-1, 79481-0043-01
- Manufacturer
- Meijer Distribution | Jell Pharmaceuticals
- Effective date
- 2024-07-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Meijer Medicated Foot Powder - Meijer Distribution | Jell Pharmaceuticals | Meijer Distribution | Jell Pharmaceuticals | 2024-07-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0043-1 | Meijer Medicated Foot Powder | 283 g in 1 BOTTLE | POWDER | 283 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0043 | MEIJER MEDICATED FOOT POWDER (MENTHOL) POWDER [MEIJER DISTRIBUTION] | 2 | Current NDC, 1 package rows | 20240730_07ec6c20-73c4-e5e4-e063-6294a90a7e55.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.