FDA.reportPublic FDA data

NDC 51688-6002-2 - 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
Requested NDC
51688-6002-2
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 17 of 129 · 2,572 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DYNA-HEX 2CHLORHEXIDINE GLUCONATEXttrium Laboratories, Inc.6cc89ac1-baef-40bb-85a3-d9ae9e3e7a632026-04-27WarningsExact identifier
unii: MOR84MUD8E
Sodium ChlorideSODIUM CHLORIDESportpharm LLCa2c111f6-74d5-4a5d-82ac-d0f237488cb82026-04-24Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
LidocaineLIDOCAINE HYDROCHLORIDESportpharm LLCcffda6fc-7e85-4c48-9623-2551d3552d7d2026-04-24Warnings, Adverse reactionsExact identifier
rxcui: 1010033
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDECamber Pharmaceuticals, Inc.7f202319-effa-4dd8-b871-e720b75f4a832026-04-23Warnings, Adverse reactionsExact identifier
rxcui: 1737757
rxcui: 1737562
rxcui: 1737566
rxcui: 1737568
unii: EC2CNF7XFP
Sodium ChlorideSODIUM CHLORIDEMethod Pharmaceuticals, LLC4b08859e-65bd-8255-e063-6394a90af6142026-04-23WarningsExact identifier
unii: 451W47IQ8X
AKTENLIDOCAINE HYDROCHLORIDE ANHYDROUSThea Pharma Inc.70ff9fb7-d323-4fe6-b1b1-6033e05f07492026-04-23Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEBryant Ranch Prepack850bdb6a-85d9-441d-8666-7a61311386b62026-04-23Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
3M DuraPrep SurgicalIODINE POVACRYLEX AND ISOPROPYL ALCOHOLSolventum US LLC22a10a54-6a04-48b3-9ec4-b26526183daf2026-04-23WarningsExact identifier
unii: ND2M416302
LIDOCAINELIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATEHenry Schein Inc.1ca96c77-d983-496b-84a6-54709e80f5322026-04-23Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LidocaineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATEHenry Schein Inc.f8d90500-f797-4238-8dd2-b59cbcd89d122026-04-23Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
3M SoluPrep SCHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOLSolventum US LLC084aa305-5863-441a-a94d-36bc1b05195a2026-04-23WarningsExact identifier
rxcui: 858726
unii: MOR84MUD8E
unii: ND2M416302
Lidocaine Hydrochloride and EpinephrineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINESportpharm LLC2c58deba-dbb2-4e73-a173-36053536f03e2026-04-22Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
3M AvagardCHLORHEXIDINE GLUCONATE AND ALCOHOLSolventum US LLC8bf8fe8e-76cb-4eda-a18d-1687050285ae2026-04-22WarningsExact identifier
unii: MOR84MUD8E
LidocaineLIDOCAINE HYDROCHLORIDESportpharm LLC7adb9ab0-ef91-4c51-baa3-a0b7e12df0772026-04-21Warnings, Adverse reactionsExact identifier
rxcui: 1010033
unii: V13007Z41A
LIDOCAINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDEBryant Ranch Prepack8f79b023-9bd1-4bd6-8fd0-f9efe88abec02026-04-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
RingersSODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEICU Medical, Inc.a926f913-18fa-4a3e-bfd6-210e1e4279602026-04-20Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Cardioforce IIABROTANUM, BOLDO, CIMICIFUGA RACEMOSA, KALI PHOSPHORICUM, TARAXACUM OFFICINALE, CONVALLARIA MAJALIS, MAGNESIA SULPHURICA, OLEANDER, NATRUM MURIATICUM, BELLIS PERENNISBioActive Nutritional, Inc.733bbb26-7698-4a1b-9dc8-7e3490ffc92b2026-04-17WarningsExact identifier
unii: 451W47IQ8X
Thyroid HPBARYTA CARBONICA, CALCAREA CARBONICA, FUCUS VESICULOSUS, IODIUM, NATRUM MURIATICUM, PULSATILLA, SPONGIA TOSTA, THYROIDINUM (SUIS)BioActive Nutritional, Inc.3795820a-cf2a-4094-9a02-70e3757b75102026-04-17WarningsExact identifier
unii: 451W47IQ8X
DIANEAL Low Calcium with DextroseSODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSEVantive US Healthcare LLCaa268d3f-7389-4f25-801f-5d4825495f082026-04-16Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Burn CreamBENZALKONIUM CHLORIDE, LIDOCAINE HCIProstat First Aid4f9adbac-5497-e7be-e063-6294a90a75182026-04-16WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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