NDC 62717-4320 - Accel Oxy
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
- 62717-4320
- Package NDCs from labels
- 62717-4320-2, 62717-4320-3, 62717-4320-4, 62717-4320-1
- 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 Oxy - 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 |
|---|---|---|---|---|---|
| HYDROGEN PEROXIDE | ACTIVE INGREDIENT | BBX060AN9V | ACCEL OXY (HYDROGEN PEROXIDE) LIQUID [ACCELERATED GENETICS] | 1 | |
| HYDROGEN PEROXIDE | ACTIVE MOIETY | BBX060AN9V | ACCEL OXY (HYDROGEN PEROXIDE) LIQUID [ACCELERATED GENETICS] | 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.