NDC 79481-0612-01 - Liquid Corn and Callus Remover
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
- 79481-0612
- Requested NDC
- 79481-0612-01
- Package NDCs from labels
- 79481-0612-1, 79481-0612-01
- Manufacturer
- Meijer Distribution Inc
- Effective date
- 2025-10-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Liquid Corn and Callus Remover - Meijer Distribution Inc | Meijer Distribution Inc | 2025-10-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0612-1 | Liquid Corn and Callus Remover | 9.8 mL in 1 BOTTLE | LIQUID | 9.8 | 5 | |
| 79481-0612-1 | Liquid Corn and Callus Remover | 1 in 1 BLISTER PACK | LIQUID | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0612 | LIQUID CORN AND CALLUS REMOVER (SALICYLIC ACID) LIQUID [MEIJER DISTRIBUTION INC] | 4 | Current NDC, 2 package rows | 20241016_039c3dbe-97ba-805c-e063-6394a90a91e8.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.