NDC 55651-031 - Biomedic Artificial Tears
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
- 55651-031
- Package NDCs from labels
- 55651-031-01
- Manufacturer
- KC Pharmaceuticals, Inc.
- Effective date
- 2025-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Biomedic Artificial Tears 15mL (MFR - EXPORT) | KC Pharmaceuticals, Inc. | 2025-12-31 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55651-031-01 | Biomedic Artificial Tears | 1 in 1 CARTON | LIQUID | 1 | 2 | |
| 55651-031-01 | Biomedic Artificial Tears | 15 mL in 1 BOTTLE, PLASTIC | LIQUID | 15 | 2 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.