FDA.reportPublic FDA data

NDC 51688-6424 - A4094 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
51688-6424
Package NDCs from labels
51688-6424-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | CareFusion 213 LLC
Effective date
2014-04-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
LIDOCAINE - Smiths Medical ASD, Inc. | Hospira, Inc. | CareFusion 213 LLCSmiths Medical ASD, Inc. | Hospira, Inc. | CareFusion 213 LLC2014-04-07MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHLORHEXIDINE GLUCONATEACTIVE INGREDIENTMOR84MUD8EA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M416302A4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41AA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
CHLORHEXIDINEACTIVE MOIETYR4KO0DY52LA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
ISOPROPYL ALCOHOLACTIVE MOIETYND2M416302A4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
LIDOCAINEACTIVE MOIETY98PI200987A4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8A4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4
WATERINACTIVE INGREDIENT059QF0KO0RA4094 NERVE BLOCK () KIT [SMITHS MEDICAL ASD, INC.]4

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 67 of 121 · 2,414 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LidotholLIDOCAINE HCL, MENTHOLClinic Pharma3159db23-6439-7c2e-e063-6294a90a310b2025-03-27Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LidocaineLIDOCAINE HYDROCHLORIDEFresenius Kabi USA, LLCcddb2b22-fce3-8967-6e54-dca3df5ac4b32025-03-26Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Sodium ChlorideSODIUM CHLORIDE TABLETBelleview Bioscience LLC31195e8f-d4de-9e37-e063-6294a90a41562025-03-24WarningsExact identifier
unii: 451W47IQ8X
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEPreferred Pharmaceuticals Inc.abf60c5c-66df-4894-aa8f-bf770a6e9d002025-03-24Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Pituitary LiquescenceCAULOPHYLLUM THALICTROIDES, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, PINEAL GLAND (SUIS), CIMICIFUGA RACEMOSA, NATRUM MURIATICUM, CINCHONA OFFICINALIS, ADRENOCORTICOTROPHINNutritional Specialties, Inc.292ca967-abe8-4ae1-b2fe-942531a1e14a2025-03-20WarningsExact identifier
unii: 451W47IQ8X
SaniiswabISOPROPYL ALCOHOLPOLLEY MED LLC303b1ad5-a104-3479-e063-6294a90abcde2025-03-20WarningsExact identifier
unii: ND2M416302
Chlorhexidine Gluconate, 0.12% Oral RinseCHLORHEXIDINE GLUCONATE, 0.12% ORAL RINSEAmerican Health Packaging21002357-1780-4a5d-ad54-9936f4a9c0312025-03-20Warnings, Adverse reactionsExact identifier
unii: MOR84MUD8E
Lignospan StandardLIDOCAINE HYDROCHLORIDE AND EPINEPHRINESeptodont, Inc.f902d2b4-28fc-41b1-a9f7-0d1a63c598aa2025-03-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lignospan ForteLIDOCAINE HYDROCHLORIDE AND EPINEPHRINESeptodont, Inc.f8ca7d03-01c8-450f-9279-59789c3497ea2025-03-20Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Anxiety HPACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, CALCAREA CARBONICA, IGNATIA AMARA, KALI CARBONICUM, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STAPHYSAGRIA, STRAMONIUMEnergique, Inc.191393fa-5f36-43c0-a183-09258eef9bda2025-03-20WarningsExact identifier
unii: 451W47IQ8X
HYDRA NEBSODIUM CHLORIDEVenture Healthcare Ltd30b184bf-2451-d96b-e063-6294a90a43c72025-03-19WarningsExact identifier
unii: 451W47IQ8X
HYDRA NEBSODIUM CHLORIDELaboratoire Unither30b244c0-84bb-a0a0-e063-6394a90a9dee2025-03-19WarningsExact identifier
unii: 451W47IQ8X
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDENuCare Pharmaceuticals,Inc.037764d3-da0e-5ebb-e063-6294a90ab6e02025-03-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
XeroBurn Burn GelLIDOCAINE HYDROCHLORIDEDynarex Corporation58985046-ca9c-12be-e053-2991aa0abe722025-03-13WarningsExact identifier
unii: V13007Z41A
Psora MiasmEGGSHELL MEMBRANE, WHEY PROTEIN, CALCAREA CARBONICA, LYCOPODIUM CLAVATUM, SULPHUR, ARSENICUM ALBUM, CROTON TIGLIUM, GRAPHITES, HYDROCOTYLE ASIATICA, NATRUM MURIATICUMEnergique, Inc.6a12aa49-35fc-41f4-bec8-6f9a20a97caa2025-03-13WarningsExact identifier
unii: 451W47IQ8X
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDENovagenix Labs LLC7567ffb5-953a-4be9-9a02-c5a50dcd93062025-03-12Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
LidocaineLIDOCAINE HYDROCHLORIDEARMAS PHARMACEUTICALS INC.2f6e0f3d-ceaf-a853-e063-6394a90a8efb2025-03-07Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Bestmade Natural Products BM253CALC FLUOR, CALC PHOS, FERR PHOS, KALI MUR, KALI PHOS, MAG PHOS, NAT MURBestmade Natural Products2fa9913f-0593-f77b-e063-6394a90ab6b22025-03-06WarningsExact identifier
unii: 451W47IQ8X
Bestmade Natural Products BM254APIS MEL, BRYONIA, GELSEMIUM, NAT MUR, PULSATILLABestmade Natural Products2fa9bb2c-848b-06ef-e063-6394a90ad0f02025-03-06WarningsExact identifier
unii: 451W47IQ8X
Medicated Foaming FeminineLACTIC ACID, BORIC ACID, CHLORHEXIDINE GLUCONATE, CNIDIUM MONNIERI FRUIT, LEVOMENOLRida LLC02b3d683-05b0-4075-bbf9-e6d97c61765c2025-03-06WarningsExact identifier
unii: MOR84MUD8E

Reported adverse events (FAERS/openFDA)#

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