FDA.reportPublic FDA data

NDC 51688-6475 - A4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE

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
51688-6475
Package NDCs from labels
51688-6475-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd.
Effective date
2015-06-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
A4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRESmiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd.2015-06-26MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EPINEPHRINEACTIVE INGREDIENTYKH834O4BHA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41AA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8XA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
EPINEPHRINEACTIVE MOIETYYKH834O4BHA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
LidocaineACTIVE MOIETY98PI200987A4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
SODIUM CATIONACTIVE MOIETYLYR4M0NH37A4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
SODIUM METABISULFITEINACTIVE INGREDIENT4VON5FNS3CA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3
WATERINACTIVE INGREDIENT059QF0KO0RA4151-17/25 COMBINED SPINAL/EPIDURAL 17G TUOHY/25G WHITACRE () KIT [SMITHS MEDICAL ASD, INC.]3

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 96 · 1,917 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TopCare Pain Relief Maximum StrengthLIDOCAINE HYDROCHLORIDETOPCO ASSOCIATESb0ae3a7c-52d1-4923-bd50-6bb3749006c82025-11-11WarningsExact identifier
unii: V13007Z41A
ComfortcaineLIDOCAINE HCLQS Key West Aloe, LLC831b7c11-e437-4e74-808e-c9c1eb8b82f62025-11-11WarningsExact identifier
unii: V13007Z41A
DermaNumb AnalgesicLIDOCAINE HCLA.T.S. Laboratories, LLC0ea46890-45c3-4732-bc47-227f7c67daf12025-11-11WarningsExact identifier
unii: V13007Z41A
Derma Numb Pain ReliefLIDOCAINE HCLA.T.S. Laboratories, LLC710991ae-8f82-4893-93a7-0ef3f815d1322025-11-11WarningsExact identifier
unii: V13007Z41A
SODIUM CHLORIDESODIUM CHLORIDEHospira, Inc.af6aebad-ef03-4d19-9a40-18e5a278b8122025-11-11Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEEugia US LLC5524cbfd-d6e6-42eb-aaa5-22495e0a86b62025-11-11Warnings, Adverse reactionsExact identifier
unii: V13007Z41A
EpinephrineEPINEPHRINEA-S Medication Solutionsab5e23d0-6e99-4647-838d-23a4040602b52025-11-10Warnings, Adverse reactionsExact identifier
unii: YKH834O4BH
Jelcaine SterileLIDOCAINE HCL JELLY USP, 2%Brookfield Pharmaceuticals, LLC1a39d1de-7aa2-3068-e063-6394a90aed852025-11-10WarningsExact identifier
unii: V13007Z41A
GuruNanda Pain ReliefLIDOCAINE HYDROCHLORIDEGuruNanda, LLC.3ab6a133-8dca-e14e-e063-6394a90a85e72025-11-10WarningsExact identifier
unii: V13007Z41A
GURUNANDA NASAL SALINENASAL WASHGURUNANDA LLC27dbf0bf-c273-2108-e063-6394a90a0a092025-11-10WarningsExact identifier
unii: 451W47IQ8X
AZO Yeast PlusCANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, AND SULFURi-Health, Inc.22845cac-8011-4ea8-b35e-b72973eddb442025-11-07WarningsExact identifier
unii: 451W47IQ8X
Genuine First Aid Pain Relieving CreamBENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDEGFA Production (Xiamen) Co., Ltd.48867a79-4d21-4ba1-9cf9-7839352a4b7e2025-11-07WarningsExact identifier
unii: V13007Z41A
SODIUM CHLORIDESODIUM CHLORIDEHenry Schein, Inc.2e81ffca-05c6-4fa0-8911-4b3cbfa713512025-11-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDERising Pharma Holdings, Inc.42870188-b1d7-4934-a6c0-310530497dac2025-11-07WarningsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEHenry Schein, Inc.d8b8d796-bfba-42af-a859-99d7768715582025-11-07Adverse reactionsExact identifier
unii: 451W47IQ8X
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Bacteriostatic Sodium ChlorideSODIUM CHLORIDEHenry Schein, Inc.31188cdf-7bc8-4d78-bfaf-c1dc9f851fd42025-11-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.d3d29c8f-c326-4097-814a-7f4e08c670682025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, AND POTASSIUM CHLORIDEB. Braun Medical Inc.01721071-af03-4894-95c1-10b8bc64b8882025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Pain Relieving CleansingBENZALKONIUM CHLORIDE, LIDOCAINE HCLTARGET CORPORATION944b3f78-3efa-484b-84f0-00ffe95c5dfb2025-11-05WarningsExact identifier
unii: V13007Z41A

Reported adverse events (FAERS/openFDA)#

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