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 13 of 129 · 2,572 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM Nat Mur Icing SugarNATRUM MURIATICUM ICING SUGARTotal Operations Management LLC DBA:Bestmade Natural Products Micro5356d350-1325-7299-e063-6294a90a96a02026-06-03WarningsExact identifier
unii: 451W47IQ8X
OP First Aid Series Insect Sting Relief PadBENZOCAINE, ISOPROPYL ALCOHOLYiwu Ori-Power Medtech Co.,Ltd.b43af183-834a-0f64-e053-2995a90a32182026-06-03WarningsExact identifier
unii: ND2M416302
PURE PRIMAL DELAYLIDOCAINE HCLProdigy Media Inc1ddab664-7c44-452f-854f-e386cd69505e2026-06-03WarningsExact identifier
unii: V13007Z41A
OptiSource Sterile Alcohol Prep PadsISOPROPYL ALCOHOL7051395 Canada Ince49c9ddf-7743-443e-ba85-ee90785f0c722026-06-02WarningsExact identifier
unii: ND2M416302
Major Oral Rinse0.12% CHLORHEXIDINE GLUCONATECardinal Health 107, LLCbaad6ebb-ba44-4abe-8882-f2391d17d8162026-05-29Warnings, Adverse reactionsExact identifier
unii: MOR84MUD8E
Aspercreme with Lidocaine No-Mess ApplicatorLIDOCAINE HYDROCHLORIDEChattem, Inc.8092cde7-28d0-4755-b5c0-5765934e572f2026-05-29WarningsExact identifier
unii: V13007Z41A
LidotholLIDOCAINE HCL, MENTHOLASCLEMED USA INC.4e2fad18-13f1-4e61-86db-d721029287172026-05-28Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
First Aid Antiseptic Pain Relieving CreamBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEHubei Fanjian Medical Product Co.,Ltdf44aa5a9-45e2-b890-e053-2a95a90a421b2026-05-28WarningsExact identifier
unii: V13007Z41A
PlegisolPOTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDEHospira, Inc.35a174f0-f0d7-4ec7-3f81-d3d572c059cf2026-05-27Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Antibacterial Lidocaine Wound GelBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDECVS Pharmacy960bfe55-87f6-3e51-e053-2995a90a867d2026-05-27WarningsExact identifier
unii: V13007Z41A
myDerm MEDICAL NEW Soothing HemorrhoidalWITCH HAZEL PENYLEPHRINE LIDOCAINEInspec Solutions2ff42501-7730-42de-99dd-6fc53bbdf25f2026-05-27WarningsExact identifier
unii: V13007Z41A
MyMedic Sting Relief WipeBENZOCAINE, ISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltd52b5653e-289c-d99e-e063-6294a90aa6472026-05-26WarningsExact identifier
unii: ND2M416302
MyDerm Aloe and LidocaineLIDOCAINEMedline Industriesfdfd4388-cd27-467b-959b-249a49ea5cf62026-05-26WarningsExact identifier
unii: V13007Z41A
MyDerm Aloe and LidocaineLIDOCAINEInspec Solutions LLC.4939c663-a876-4527-822a-df02964fa6942026-05-26WarningsExact identifier
unii: V13007Z41A
TPN ElectrolytesSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, AND SODIUM ACETATE ANHYDROUSHospira, Inc.c00817bc-7b62-4abe-0280-e7930eda3f942026-05-25Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Swab Applicator Brushes 4% w/w chlorhexidine gluconate (CHG)CHLORHEXIDINE GLUCONATEXINXIANG XINDA TECHNOLOGY CO.,LTD51c1a74f-c6a8-b831-e063-6294a90a6c712026-05-24WarningsExact identifier
unii: MOR84MUD8E
Swab Applicator Brushes 8.3% w/w Povidone-Iodine and 72.5% w/w Isopropyl Alcohol (IPA)POVIDONE-IODINE, ISOPROPYL ALCOHOLXINXIANG XINDA TECHNOLOGY CO.,LTD529b8ad6-081e-0ef8-e063-6294a90a67df2026-05-24WarningsExact identifier
unii: ND2M416302
Swab Stick 2% w/w chlorhexidine gluconate (CHG) and 70% v/v isopropyI alcohol (IPA)CHLORHEXIDINE GLUCONATE, ISOPROPYI ALCOHOLXINXIANG XINDA TECHNOLOGY CO.,LTD51c42761-3a7a-172d-e063-6394a90a53332026-05-24WarningsExact identifier
unii: MOR84MUD8E
unii: ND2M416302
Swab Stick 2% w/w chlorhexidine gluconate (CHG)CHLORHEXIDINE GLUCONATEXINXIANG XINDA TECHNOLOGY CO.,LTD51c5a926-d137-9119-e063-6294a90a88452026-05-24WarningsExact identifier
unii: MOR84MUD8E
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHospira, Inc.89a4bd73-89f4-4fd7-2c9f-921e1da8f96b2026-05-22Warnings, Adverse reactionsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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