NDC 55553-482 - ACL11CH NERVE BLOCK
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
- 55553-482
- Package NDCs from labels
- 55553-482-02
- Manufacturer
- Smiths Medical ASD, Inc. | CareFusion 213 LLC
- Effective date
- 2014-04-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ACL11CH NERVE BLOCK - Smiths Medical ASD, Inc. | CareFusion 213 LLC | Smiths Medical ASD, Inc. | CareFusion 213 LLC | 2014-04-14 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54365-400-11 | ACL11CH NERVE BLOCK | 3 mL in 1 APPLICATOR | SOLUTION | 3 mL | 20 mg in 1mL | 1 |
| 55553-482-02 | ACL11CH NERVE BLOCK | 1 in 1 PACKAGE, COMBINATION | KIT | 1 | 1 | |
| 55553-482-02 | ACL11CH NERVE BLOCK | 30 in 1 CASE | KIT | 30 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CHLORHEXIDINE GLUCONATE | ACTIVE INGREDIENT | MOR84MUD8E | ACL11CH NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| ISOPROPYL ALCOHOL | ACTIVE INGREDIENT | ND2M416302 | ACL11CH NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| CHLORHEXIDINE | ACTIVE MOIETY | R4KO0DY52L | ACL11CH NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| ISOPROPYL ALCOHOL | ACTIVE MOIETY | ND2M416302 | ACL11CH NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | ACL11CH NERVE BLOCK () 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.