NDC 15455-9569 - LuraDRox Rx Wound Gel
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
- 15455-9569
- Package NDCs from labels
- 15455-9569-1
- Manufacturer
- Alvix Laboratories
- Effective date
- 2019-03-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| LuraDRox Rx Wound Gel - Alvix Laboratories | Alvix Laboratories | 2019-03-27 | PRESCRIPTION MEDICAL DEVICE LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 15455-9569-1 | ML - Milliliter | 15455-9569 | 3613f2f7-c2e1-45dc-a36d-d9c4ff8968ba | 1 | 2019-04-11 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.