NDC 51688-6002 - Nerve Block A3769
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
- 51688-6002
- Package NDCs from labels
- 51688-6002-2
- Manufacturer
- Smiths Medical ASD, Inc. | CareFusion 213 LLC | Hospira, Inc.
- Effective date
- 2011-04-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nerve Block A3769 | Smiths Medical ASD, Inc. | CareFusion 213 LLC | Hospira, Inc. | 2011-04-06 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
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.
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| Antiseptic Skin Cleanser | CHLORHEXIDINE GLUCONATE 4% | Chain Drug Marketing Association Inc. | 12234b17-fd07-6088-e054-00144ff88e88 | 2025-12-12 | Warnings | MOR84MUD8E |
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| ANTISEPTIC SKIN CLEANSER | CHLORHEXIDINE GLUCONATE | Xttrium Laboratories, Inc. | 9f6342f7-faa3-4d23-a860-054d04cb8d42 | 2025-12-10 | Warnings | MOR84MUD8E |
| ALCOH-WIPE | ISOPROPYL ALCOHOL | Veltek Associates, Inc. | 343ba13e-7f90-5dab-e063-6294a90a56ae | 2025-12-10 | Warnings | ND2M416302 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.