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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Dukal Sterile Alcohol Prep Pad | ISOPROPYL ALCOHOL | Dukal Corporation | 54586d75-a0a1-46aa-9cc9-631094320bff | 2019-02-28 | Warnings | ND2M416302 |
| CHLORHEXIDINE GLUCONATE | CHLORHEXIDINE GLUCONATE | Lyne Laboratories, Inc. | 0348006f-b818-4465-a896-bc0d42294cf4 | 2019-01-02 | Warnings, Adverse reactions | MOR84MUD8E |
| Dynamic Eyewash with Eyecup | WATER | Dynamic Safety International | 7d3af0f4-0e1f-9ea5-e053-2991aa0af7a2 | 2018-12-17 | Warnings | 059QF0KO0R |
| Antimicrobial Foam Handwash | CHLORHEXIDINE GLUCONATE 2% SOLUTION | GOJO Industries, Inc. | 743021cd-38c3-3825-e053-2a91aa0aa7f2 | 2018-08-24 | Warnings | MOR84MUD8E |
| Antiseptic Foam Handwash | CHLORHEXIDINE GLUCONATE 2% SOLUTION | GOJO Industries, Inc. | 74317b4d-3fbf-6fd5-e053-2a91aa0ab90f | 2018-08-24 | Warnings | MOR84MUD8E |
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| ANTISEPTIC SKIN CLEANSER | CHLORHEXIDINE GLUCONATE | Xttrium Laboratories, Inc. | 6e62eb50-ebaa-361e-e053-2991aa0aba6f | 2018-06-11 | Warnings | MOR84MUD8E |
| ENT Essentials All Dry Ear Drying Drops | ISOPROPYL ALCOHOL | Wisconsin Pharmacal Company | 5f0bb412-577e-3155-e053-2a91aa0a7f53 | 2017-11-28 | Warnings | ND2M416302 |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Hand Wipes | CHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 181e5fa0-ddda-4783-a0b5-ff95bfce6b36 | 2017-10-09 | Warnings | MOR84MUD8E |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.