NDC 51688-6025 - PORTEX NERVE BLOCK A3632
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
- 51688-6025
- Package NDCs from labels
- 51688-6025-2
- Manufacturer
- Smiths Medical ASD, Inc. | CareFusion 213 LLC
- Effective date
- 2011-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PORTEX NERVE BLOCK A3632 - Smiths Medical ASD, Inc. | CareFusion 213 LLC | Smiths Medical ASD, Inc. | CareFusion 213 LLC | 2011-06-03 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CHLORHEXIDINE GLUCONATE | ACTIVE INGREDIENT | MOR84MUD8E | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 2 | |
| ISOPROPYL ALCOHOL | ACTIVE INGREDIENT | ND2M416302 | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 2 | |
| CHLORHEXIDINE | ACTIVE MOIETY | R4KO0DY52L | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 2 | |
| ISOPROPYL ALCOHOL | ACTIVE MOIETY | ND2M416302 | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 2 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 2 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | PORTEX NERVE BLOCK (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 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.