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 55 of 71 · 1,402 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eye WashWATERJiangxi Zhenmei Biological Technology Co.,Ltdc68795b8-bf68-0d01-e053-2a95a90abebb2023-12-04WarningsExact identifier
unii: 059QF0KO0R
XylocaineLIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATEA-S Medication Solutions38610ee9-4e70-4a8a-a5c5-6c148cf145f02023-12-04Warnings, Adverse reactionsExact identifier
unii: EC2CNF7XFP
terrasil Eczema and Psoriasis Severe OutbreakGRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIGAidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions4d7128fb-57f1-4d0d-a83a-daef40928ecd2023-11-30WarningsExact identifier
unii: 451W47IQ8X
terragen HG Formula Maximum StrengthGRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIGAidance Scientific, Inc, DBA Aidance Skincare & Topical Solutionse632c831-e25d-4d04-ba72-2327d25713b12023-11-30WarningsExact identifier
unii: 451W47IQ8X
Femstat CECHINACEA (ANGUSTIFOLIA), FUCUS VESICULOSUS, HYDRASTIS CANADENSIS, PHYTOLACCA DECANDRA, KREOSOTUM, NATRUM MURIATICUM, CANDIDA ALBICANS, LYCOPODIUM CLAVATUM, PULSATILLA (PRATENSIS), SEPIAEnergique, Inc.420119ca-f2bf-40e3-9e40-00498724c2282023-11-30WarningsExact identifier
unii: 451W47IQ8X
PhexxiLACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATEEvofem, Inc.173ff411-7227-47b0-94dc-844e1ebaf14e2023-11-21Warnings, Adverse reactionsExact identifier
unii: 2968PHW8QP
EndoparGLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, OOPHORINUM (SUIS), ORCHITINUM (BOVINE), PINEAL GLAND, THYROIDINUM, ARSENICUM ALBUM, BARYTA CARBONICA, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PULSATILLA (PRATENSIS)Energique, Inc.06375c3e-cc05-4450-9117-1d3dc72636eb2023-11-21WarningsExact identifier
unii: 451W47IQ8X
Prep non sterilePOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltdecbe037b-77da-4ffc-8c60-e56f428766af2023-11-15WarningsExact identifier
unii: 85H0HZU99M
Prep Pad SterilePOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd758abf53-ad8a-62ac-e053-2991aa0a8f0c2023-11-15WarningsExact identifier
unii: 85H0HZU99M
Natrum muriaticumSODIUM CHLORIDEBoiron8646d7ea-cf5e-607d-e053-2a91aa0aeca12023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86466121-7217-d053-e053-2a91aa0a8f8a2023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron864669c9-5bdc-232f-e053-2a91aa0a1fc62023-11-14Exact identifier
unii: 451W47IQ8X
Natrum muriaticumSODIUM CHLORIDEBoiron86462e06-d221-36b7-e053-2991aa0a1d822023-11-14Exact identifier
unii: 451W47IQ8X
Maokang Povidone Iodine Swabsticks 3sPOVIDONE-IODINEChangzhou Maokang Medical Products Co.,Ltd15443c2d-b531-4635-8d0c-53057bee0db72023-11-14WarningsExact identifier
unii: 85H0HZU99M
TWO PVP-I SCRUB STICKSPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd88bee1c7-0d6d-46b7-8dce-ce05aa0388fa2023-11-10WarningsExact identifier
unii: 85H0HZU99M
TWO PVP-I SCRUB LARGE WINGED SPONGESPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd4295c0c5-6be0-4d0f-9456-a92e3571d6792023-11-10WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine Scrub SterilePOVIDONE-IODINECardinal Health 200 LLC66146848-aec8-466f-b993-6b8e3318165d2023-11-10WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine Prep SterilePOVIDONE-IODINECardinal Health 200 LLCafc2b2c2-046b-4319-b0b8-cf6d7a74b5f62023-11-10WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine Prep Winged Sterile LargePOVIDONE-IODINECardinal Health 200, Inc1a19eee2-d023-4fca-9564-d49b45fe656f2023-11-10WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine Paint SolutionPOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltd9299d5a9-40b4-4a71-bcba-91e422731e662023-11-10WarningsExact identifier
unii: 85H0HZU99M

Reported adverse events (FAERS/openFDA)#

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