NDC 86002-105 - TrisOphtho
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
- 86002-105
- Package NDCs from labels
- 86002-105-00, 86002-105-50
- Manufacturer
- DermaZoo, LLC
- Effective date
- 2015-03-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TrisOphtho - DermaZoo, LLC | DermaZoo, LLC | 2015-03-23 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CHLORHEXIDINE GLUCONATE | ACTIVE INGREDIENT | MOR84MUD8E | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| CHLORHEXIDINE | ACTIVE MOIETY | R4KO0DY52L | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| BENZALKONIUM CHLORIDE | INACTIVE INGREDIENT | F5UM2KM3W7 | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| EDETIC ACID | INACTIVE INGREDIENT | 9G34HU7RV0 | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| TROMETHAMINE | INACTIVE INGREDIENT | 023C2WHX2V | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| TROMETHAMINE HYDROCHLORIDE | INACTIVE INGREDIENT | 383V75M34E | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | TRISOPHTHO (CHLORHEXIDINE GLUCONATE) LIQUID [DERMAZOO, LLC] | 2 |
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.