NDC 59399-162 - 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
- 59399-162
- Package NDCs from labels
- 59399-162-35
- Manufacturer
- Akorn | Croda Europe Ltd.
- Effective date
- 2022-11-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Artificial Tears - Akorn | Croda Europe Ltd. | Akorn | Croda Europe Ltd. | 2022-11-03 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59399-162-35 | Artificial Tears | 1 in 1 CARTON | OINTMENT | 1 | 4 | |
| 59399-162-35 | Artificial Tears | 3.5 g in 1 TUBE | OINTMENT | 3.5 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Mineral Oil | ACTIVE INGREDIENT | T5L8T28FGP | ARTIFICIAL TEARS (MINERAL OIL AND WHITE PETROLATUM) OINTMENT [AKORN ANIMAL HEALTH, INC.] | 1 | |
| Petrolatum | ACTIVE INGREDIENT | 4T6H12BN9U | ARTIFICIAL TEARS (MINERAL OIL AND WHITE PETROLATUM) OINTMENT [AKORN ANIMAL HEALTH, INC.] | 1 | |
| Mineral Oil | ACTIVE MOIETY | T5L8T28FGP | ARTIFICIAL TEARS (MINERAL OIL AND WHITE PETROLATUM) OINTMENT [AKORN ANIMAL HEALTH, INC.] | 1 | |
| Petrolatum | ACTIVE MOIETY | 4T6H12BN9U | ARTIFICIAL TEARS (MINERAL OIL AND WHITE PETROLATUM) OINTMENT [AKORN ANIMAL HEALTH, INC.] | 1 | |
| Lanolin | INACTIVE INGREDIENT | 7EV65EAW6H | ARTIFICIAL TEARS (MINERAL OIL AND WHITE PETROLATUM) OINTMENT [AKORN ANIMAL HEALTH, INC.] | 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.