NDC 51688-9507 - 15240-20 SINGLE SHOT EPIDURAL 20G LUTZ

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
51688-9507
Package NDCs from labels
51688-9507-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd. | Aplicare, Inc.
Effective date
2015-02-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
15240-20 SINGLE SHOT EPIDURAL 20G LUTZSmiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd. | Aplicare, Inc.2015-02-04MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41A15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99M15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
CHLORIDE IONACTIVE MOIETYQ32ZN4869815240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
IODINEACTIVE MOIETY9679TC07X415240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
LIDOCAINEACTIVE MOIETY98PI20098715240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CB15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9T15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8X15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
Sodium HydroxideINACTIVE INGREDIENT55X04QC32I15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA7415240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2
WaterINACTIVE INGREDIENT059QF0KO0R15240-20 SINGLE SHOT EPIDURAL 20G LUTZ () KIT [SMITHS MEDICAL ASD, INC.]2

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 77 of 97 · 1,940 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HEB Povidone IodinePOVIDONE IODINE 10%H E B5d576ce2-7d63-c860-e053-2a91aa0a072c2023-12-18WarningsExact identifier
unii: 85H0HZU99M
Publix Povidone IodinePOVIDONE IODINE 10%Publix5d6bba46-2571-4957-e053-2a91aa0a2e852023-12-18WarningsExact identifier
unii: 85H0HZU99M
DermaWound Wound CarePOVIDONE-IODINEProgressive Doctors, LLC2d49daa7-aa02-4219-880b-e1697bde8a7e2023-12-15WarningsExact identifier
unii: 85H0HZU99M
Povidone IodinePOVIDONE-IODINE SPRAY 5%Humco Holding Group, Inc.a7bb80c4-bbc0-21ea-e053-2995a90a52c12023-12-15WarningsExact identifier
unii: 85H0HZU99M
Povidone IodinePOVIDONE IODINE 10%Humco Holding Group, Inc.6064c23b-7c15-208d-e053-2991aa0a00f62023-12-15WarningsExact identifier
unii: 85H0HZU99M
Povidone IodinePOVIDONE IODINE GARGLE 0.5%Humco Holding Group, Inc.a7b9ad55-cfeb-6066-e053-2a95a90af9752023-12-15WarningsExact identifier
unii: 85H0HZU99M
Lidocaine Pain Relief Roll-OnLIDOCAINE 4%Humco Holding Group, Inc.a8be9e46-1616-40a9-e053-2a95a90ac3bc2023-12-15WarningsExact identifier
unii: V13007Z41A
Povidone IodinePOVIDONE IODINE ORAL RINSE 0.5%Humco Holding Group, Inc.b83dbdd1-ff63-caf8-e053-2a95a90a57642023-12-15WarningsExact identifier
unii: 85H0HZU99M
Rite Aid Povidone IodinePOVIDONE IODINE 10%Rite Aid Corporation5df6ff37-a4ea-d666-e053-2991aa0a97862023-12-15WarningsExact identifier
unii: 85H0HZU99M
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHikma Pharmaceuticals USA Inc.c5d27da0-e495-4bb6-a7e1-8eaa6595eb712023-12-14Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
BSSBALANCED SALT SOLUTIONAlcon Laboratories, Inc.28488c7b-cf6a-4a03-916f-cc66b3afdc572023-12-14Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Povidone-Iodine Prep SterilePOVIDONE-IODINEChangzhou Maokang Medical Products Co., Ltdbb62784a-d7b7-471e-9aed-0c6d2e349c3a2023-12-13WarningsExact identifier
unii: 85H0HZU99M
Altachlore Sodium Chloride HypertonicitySODIUM CHLORIDEAltaire Pharmaceuticals Inc.dc0d94d8-4475-4956-8ded-bdb9496074e42023-12-09WarningsExact identifier
unii: 451W47IQ8X
OracitCITRIC ACID AND SODIUM CITRATECMP Pharma, Inc.bc26abed-8e6e-475d-8ab3-abf7d03770032023-12-07Adverse reactionsExact identifier
unii: 2968PHW8QP
Eye WashWATERJiangxi Zhenmei Biological Technology Co.,Ltdc68795b8-bf68-0d01-e053-2a95a90abebb2023-12-04WarningsExact identifier
unii: 059QF0KO0R
Lidozen GelLIDOCAINE HYDROCHLORIDE, MENTHOLProficient Rx LP7c300dec-cefd-4b79-a948-a917b7708a042023-12-01WarningsExact identifier
unii: V13007Z41A
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
Thera Plus Max Strength Lidocaine Pain Relief LiquidLIDOCAINE HYDROCHLORIDEFourstar Group USA, Inc.0a228b06-0e1c-6c75-e063-6294a90a9a0e2023-11-30WarningsExact identifier
unii: V13007Z41A
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

Reported adverse events (FAERS/openFDA)#

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