NDC 62717-4170-1 - Accel Gold Kote
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
- 62717-4170
- Requested NDC
- 62717-4170-1
- Package NDCs from labels
- 62717-4170-2, 62717-4170-3, 62717-4170-4, 62717-4170-1
- Manufacturer
- Accelerated Genetics | ProActive Solution USA, LLC
- Effective date
- 2013-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Accel Gold Kote - Accelerated Genetics | ProActive Solution USA, LLC | Accelerated Genetics | ProActive Solution USA, LLC | 2013-12-31 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BRONOPOL | ACTIVE INGREDIENT | 6PU1E16C9W | ACCEL GOLD KOTE (BRONOPOL) LIQUID [ACCELERATED GENETICS] | 1 | |
| BRONOPOL | ACTIVE MOIETY | 6PU1E16C9W | ACCEL GOLD KOTE (BRONOPOL) LIQUID [ACCELERATED GENETICS] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.