NDC 51688-6414 - A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE
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
- 51688-6414
- Package NDCs from labels
- 51688-6414-2
- Manufacturer
- Smiths Medical ASD, Inc. | Aplicare, Inc.
- Effective date
- 2013-08-28
- 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. | 2013-08-28 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POVIDONE-IODINE | ACTIVE INGREDIENT | 85H0HZU99M | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| NONOXYNOL-9 | INACTIVE INGREDIENT | 48Q180SH9T | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | A4064-22 LUMBAR PUNCTURE, INFANT 22 QUINCKE () 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.