NDC 51688-5375-2 - A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY
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
- 51688-5375
- Requested NDC
- 51688-5375-2
- Package NDCs from labels
- 51688-5375-2
- Manufacturer
- Smiths Medical ASD, Inc. | Aplicare, Inc.
- Effective date
- 2016-06-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aplicare Povidone-Iodine - Smiths Medical ASD, Inc. | Aplicare, Inc. | Smiths Medical ASD, Inc. | Aplicare, Inc. | 2016-06-20 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POVIDONE-IODINE | ACTIVE INGREDIENT | 85H0HZU99M | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| NONOXYNOL-9 | INACTIVE INGREDIENT | 48Q180SH9T | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | A3591 PORTEX REGIONAL ANESTHESIA PREP TRAY () KIT [SMITHS MEDICAL ASD, INC.] | 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.