FDA.reportPublic FDA data

NDC 51688-6006 - SINGLE SHOT EPIDURAL 22G QUINCKE A3731-22

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
51688-6006
Package NDCs from labels
51688-6006-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.
Effective date
2011-04-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SINGLE SHOT EPIDURAL 22G QUINCKE A3731-22Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.2011-04-28MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENTEC2CNF7XFPSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99MSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
IODINEACTIVE MOIETY9679TC07X4SINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
LidocaineACTIVE MOIETY98PI200987SINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9TSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA74SINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSINGLE SHOT EPIDURAL 22G QUINCKE (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]1

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 30 of 104 · 2,080 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERProPharma Distribution386a0a2f-4ff7-f128-e063-6294a90a7d4d2025-12-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution3f2c33e5-290e-2f89-e063-6394a90aee692025-12-18Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution42caf92e-6fa9-5bd7-e063-6294a90a39042025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 1010033
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution42d9e4cf-ca73-ec6d-e063-6394a90ae9372025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 1010671
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution3f2bdb1f-f1c0-370d-e063-6294a90a5c502025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 1010033
unii: V13007Z41A
Sodium ChlorideSODIUM CHLORIDEProPharma Distribution3f79fb8b-d0e8-db2a-e063-6394a90ac1362025-12-18Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lidocaine Hydrochloride and EpinephrineLIDOCAINE HYDROCHLORIDE AND EPINEPHRINEProPharma Distribution43048b6b-3c83-eef4-e063-6294a90a34cb2025-12-18Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
After Burn2.5% LIDOCAINE HCLTender Corporation d/b/a Adventure Ready Brands4640395f-a76c-d022-e063-6294a90adde62025-12-18WarningsExact identifier
unii: EC2CNF7XFP
AplicarePOVIDONE-IODINEAplicare Products LLC0a48b8ef-f2d6-ed50-e063-6394a90a8ebe2025-12-18WarningsExact identifier
unii: 85H0HZU99M
AplicarePOVIDONE IODINEAplicare Products LLC0b3e4f14-e9e6-2f2e-e063-6394a90ab2e12025-12-18WarningsExact identifier
unii: 85H0HZU99M
Aplicare Povidone-IodinePOVIDONE-IODINEAplicare Products, LLC1ad9237e-80ee-4769-ba53-9bc1bb6672492025-12-18WarningsExact identifier
unii: 85H0HZU99M
lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDEMedical Purchasing Solutions, LLC4643042c-ec95-3bad-e063-6294a90a82502025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 1010033
unii: V13007Z41A
Povidone IodinePOVIDONE-IODINETwinMed LLCfc8cb10c-4973-c0bd-e053-6394a90a6fdb2025-12-18WarningsExact identifier
unii: 85H0HZU99M
Povidone IodinePOVIDONE-IODINETwinMed LLCfcf27cbf-9535-1356-e053-6394a90a03622025-12-18WarningsExact identifier
unii: 85H0HZU99M
Povidone IodinePOVIDONE-IODINETwinMed LLCfcf30b3a-c25b-7aaf-e053-6394a90affda2025-12-18WarningsExact identifier
unii: 85H0HZU99M
Body BalanceARALIA QUIN, ARNICA, AVENA, CARDUUS MAR, ELAEIS, GLANDULA SUPRARENALIS SUIS, NAT MUR, PHOSPHORICUM AC, THUJA OCCEight and Company L.L.C876cc0cf-c7a7-4656-adf9-1eff9bb626872025-12-18WarningsExact identifier
unii: 451W47IQ8X
ZIMS MAX FREEZELIDOCAINE HYDROCHLORIDE AND MENTHOL,KOBAYASHI Healthcare International, Inc.e364ff83-4aaf-4897-a7da-06581bc321f22025-12-18WarningsExact identifier
unii: V13007Z41A
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDECardinal Health 107, LLC4e46cac7-00cd-4a01-ba11-9af4960cfbe92025-12-18Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
ADRENOPLEXCHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), GLANDULA SUPRARENALIS BOVINE, SPLEEN (SUIS), CARDUUS MARIANUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUMBioActive Nutritional, Inc.3c53c23e-7654-4e46-acf1-edb0d605ff3b2025-12-18WarningsExact identifier
unii: 451W47IQ8X
VermasodeARTEMISIA VULGARIS, CHELIDONIUM MAJUS, GRANATUM, SPIGELIA ANTHELMIA, RATANHIA, ARSENICUM ALBUM, FERRUM METALLICUM, CALCAREA CARBONICA, CINA, GAERTNER BACILLUS, GRAPHITES, MERCURIUS DULCIS, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, VERMIN NOSODENatural Creations, Inc180b5641-5692-42d4-8472-fdadccebd7462025-12-18WarningsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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