FDA.reportPublic FDA data

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 table
LabelManufacturerEffective dateType
Nerve Block A3769Smiths Medical ASD, Inc. | CareFusion 213 LLC | Hospira, Inc.2011-04-06MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHLORHEXIDINE GLUCONATEACTIVE INGREDIENTMOR84MUD8ENERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302NERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
LIDOCAINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENTEC2CNF7XFPNERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
CHLORHEXIDINEACTIVE MOIETYR4KO0DY52LNERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302NERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
LIDOCAINEACTIVE MOIETY98PI200987NERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8NERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBNERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XNERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
Sodium HydroxideINACTIVE INGREDIENT55X04QC32INERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6
WATERINACTIVE INGREDIENT059QF0KO0RNERVE BLOCK (REGIONAL ANESTHESIA) KIT [SMITHS MEDICAL ASD, INC.]6

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.

Matched openFDA labels page 36 of 95 · 1,894 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
XylocaineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINEHenry Schein, Inc.27c2e78d-d037-470d-b4fa-44c33d78f7882025-11-07Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
AZO Yeast PlusCANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, AND SULFURi-Health, Inc.22845cac-8011-4ea8-b35e-b72973eddb442025-11-07WarningsExact identifier
unii: 451W47IQ8X
SODIUM CHLORIDESODIUM CHLORIDEHenry Schein, Inc.2e81ffca-05c6-4fa0-8911-4b3cbfa713512025-11-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDERising Pharma Holdings, Inc.42870188-b1d7-4934-a6c0-310530497dac2025-11-07WarningsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEHenry Schein, Inc.d8b8d796-bfba-42af-a859-99d7768715582025-11-07Adverse reactionsExact identifier
unii: 451W47IQ8X
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
XylocaineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINEHenry Schein, Inc.6899113c-dee4-4227-9f68-475fcce6b91e2025-11-07Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
XylocaineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINEHenry Schein, Inc.cfcc8a07-b40c-476d-9a21-83487318ac852025-11-07Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
Bacteriostatic Sodium ChlorideSODIUM CHLORIDEHenry Schein, Inc.31188cdf-7bc8-4d78-bfaf-c1dc9f851fd42025-11-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
XylocaineLIDOCAINE HYDROCHLORIDEHenry Schein, Inc.ffc87dfb-0e26-4b42-80fd-3fb7690119e32025-11-07Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
XylocaineLIDOCAINE HCLHenry Schein, Inc.a6019956-a6e0-4988-a870-6aee06c354c32025-11-07Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
Pocket NurseISOPROPYL ALCOHOLPocket Nurse Enterprises, LLC42ded32e-15d9-8b03-e063-6394a90ad6bc2025-11-06WarningsExact identifier
unii: ND2M416302
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.d3d29c8f-c326-4097-814a-7f4e08c670682025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, AND POTASSIUM CHLORIDEB. Braun Medical Inc.01721071-af03-4894-95c1-10b8bc64b8882025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Dextrose in Lactated RingersDEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.190da07e-a616-46e6-b4e5-1c0ba39306e52025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.f6d82772-638c-4584-b9d3-8833669f59632025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Bacteriostatic WaterBACTERIOSTATIC WATERProPharma Distribution42c6938e-f747-ae13-e063-6294a90a59a32025-11-04Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC85291b2b-40b9-07fa-e053-2a91aa0a84e42025-11-04WarningsExact identifier
application number: NDA020832
ndc (product): 54365-400
rxcui: 858726
rxcui: 998282
spl id: 42c769de-f1e0-b3a1-e063-6394a90ab2a1
spl set id: 85291b2b-40b9-07fa-e053-2a91aa0a84e4
unii: MOR84MUD8E
unii: ND2M416302
Com-Pare2 Dual Yeast Relief Plus Multi-symptom FormulaCANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHURTRP Company42b6b9b9-a673-0bba-e063-6394a90a88662025-11-03WarningsExact identifier
unii: 451W47IQ8X
ChloraPrep One-StepCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLCareFusion 213, LLC85416361-90b5-3efa-e053-2a91aa0af4312025-11-03WarningsExact identifier
application number: NDA020832
ndc (product): 54365-400
rxcui: 858726
rxcui: 998282
spl id: 42b89ed3-8625-c3c3-e063-6294a90afa62
spl set id: 85416361-90b5-3efa-e053-2a91aa0af431
unii: MOR84MUD8E
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.