NDC 67172-362 - MURINE EAR WAX REMOVAL
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
- 67172-362
- Package NDCs from labels
- 67172-362-01
- Manufacturer
- Prestige Brands Holdings, Inc.
- Effective date
- 2025-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Murine Ear Wax Removal System_67172-362 | Prestige Brands Holdings, Inc. | 2025-10-30 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67172-362-01 | MURINE EAR WAX REMOVAL | 1 in 1 CARTON | LIQUID | 1 | 1 | |
| 67172-362-01 | MURINE EAR WAX REMOVAL | 15 mL in 1 BOTTLE, DROPPER | LIQUID | 15 | 1 |
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.