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 34 of 92 · 1,836 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
Eyewash Station Additive ConcentrateCHLORHEXIDINE GLUCONATE AND PROPYLENE GLYCOLNiagara Pharmaceuticals Inc.362a6b6d-862d-4322-87a8-5b3a07fbe1742025-11-24WarningsExact identifier
unii: MOR84MUD8E
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Natural Eyes Floaters ReliefCHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEATRP Company445dc831-195e-4b25-e063-6294a90a6efd2025-11-24WarningsExact identifier
unii: 451W47IQ8X
Lights SwabsticksISOPROPYL ALCOHOLLights Medical Manufacture Co., Ltd.4435a4e6-46ae-f49b-e063-6394a90a1d9e2025-11-22WarningsExact identifier
unii: ND2M416302
Antiseptic Skin CleanserCHLORHEXIDINE GLUCONATE 4%Xttrium Laboratories, Inc.4a68456e-4183-5371-e054-00144ff88e882025-11-21WarningsExact identifier
unii: MOR84MUD8E
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
MK Alcohol Prep Pads LargeISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltdf1ff70d7-d0f2-45db-96e9-883b54c6e4412025-11-20WarningsExact identifier
unii: ND2M416302
Vital Female Sexual EnergyAGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, ONOSMODIUM VIRGINIANUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SEPIA, THUJA OCCIDENTALISLiddell Laboratories, Inc.1ca43c82-62b0-4191-81a4-27f7f94109dd2025-11-20WarningsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEWalgreen Companyd112a344-33cc-41d3-bae6-492631ebdba72025-11-19WarningsExact identifier
unii: 451W47IQ8X
Dukal Alcohol Prep PadISOPROPYL ALCOHOLDukal LLC953b0dd6-a667-4146-815e-6845aba0309b2025-11-19WarningsExact identifier
unii: ND2M416302
Dukal Sterile Alcohol SwabstickISOPROPYL ALCOHOLDukal LLC8e47e9ad-cea4-76a4-e053-2a95a90ae7802025-11-19WarningsExact identifier
unii: ND2M416302
Sodium chlorideSODIUM CHLORIDEFresenius Kabi USA, LLCce0c8c6f-734a-400f-9b60-a3b1e263f25f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sodium ChlorideSODIUM CHLORIDE TABLETSKesin Pharma Corporation2f107592-10c5-ef3b-e063-6394a90a7c0a2025-11-17WarningsExact identifier
unii: 451W47IQ8X
Alcohol Prep PadISOPROPYL ALCOHOLShandong Lianfa Medical Plastic Products CO.,LTD435fd382-d2f5-b07f-e063-6294a90a7d8a2025-11-14WarningsExact identifier
unii: ND2M416302
BodyMed Alcohol Prep PadALCOHOL PREP PADBoxout, LLCd30dce9c-8d12-4c71-e053-2995a90a12052025-11-14WarningsExact identifier
unii: ND2M416302
ALUMIZENGARLIC, AVENA SATIVA FLOWERING TOP, BERBERIS VULGARIS ROOT BARK, ARCTIUM LAPPA ROOT, PHYTOLACCA AMERICANA ROOT, SOLIDAGO VIRGAUREA FLOWERING TOP, ALUMINUM OXIDE, SILVER NITRATE, BARIUM CARBONATE, BERYLLIUM, CADMIUM, COPPER, HYDROFLUORIC ACID, INDIUM, IODINE, LITHIUM CARBONATE, MERCURIUS SOLUBILIS, NICKEL CARBONATE HYDROXIDE TETRAHYDRATE, NITROUS OXIDE, LEAD, SELENIUM, STRONTIUM CARBONATE, TITANIUM, ARSENIC TRIOXIDE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED.Natural Creations, Inc.4760ab09-1141-4944-b840-804ae6d86d2d2025-11-13WarningsExact identifier
unii: 451W47IQ8X
Alcohol Prep PadsISOPROPYL ALCOHOLShandong Lianfa Medical Plastic Products CO.,LTD43401653-b260-e86d-e063-6294a90abb3f2025-11-13WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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