FDA.reportPublic FDA data

NDC 51688-9286 - A3211-25 SPINAL 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
51688-9286
Package NDCs from labels
51688-9286-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | 3M Company
Effective date
2015-03-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Epinephrine - Smiths Medical ASD, Inc. | Hospira, Inc. | 3M CompanySmiths Medical ASD, Inc. | Hospira, Inc. | 3M Company2015-03-12MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BUPIVACAINE HYDROCHLORIDEACTIVE INGREDIENT7TQO7W3VT8A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
EPINEPHRINEACTIVE INGREDIENTYKH834O4BHA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Iodine povacrylexACTIVE INGREDIENT6E43AWY083A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Isopropyl alcoholACTIVE INGREDIENTND2M416302A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
LIDOCAINE HYDROCHLORIDEACTIVE INGREDIENTV13007Z41AA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
BUPIVACAINEACTIVE MOIETYY8335394ROA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
EPINEPHRINEACTIVE MOIETYYKH834O4BHA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
IodineACTIVE MOIETY9679TC07X4A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Isopropyl alcoholACTIVE MOIETYND2M416302A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
LIDOCAINEACTIVE MOIETY98PI200987A3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
ANHYDROUS DEXTROSEINACTIVE INGREDIENT5SL0G7R0OKA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
SODIUM METABISULFITEINACTIVE INGREDIENT4VON5FNS3CA3211-25 SPINAL 25G WHITACRE () C47916 [SMITHS MEDICAL ASD, INC.]3
WaterINACTIVE INGREDIENT059QF0KO0RA3211-25 SPINAL 25G WHITACRE () C47916 [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 50 of 132 · 2,634 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
Isopropyl Rubbing Alcohol 70%ISOPROPYL ALCOHOLJell Pharmaceuticals Pvt. Ltd.cd9884b7-6df3-5ece-e053-2a95a90ab20e2025-11-11WarningsExact identifier
unii: ND2M416302
Isopropyl Rubbing AlcoholISOPROPYL ALCOHOLJell Pharmaceuticals Pvt. Ltd.cd8643ef-dc83-8bc1-e053-2995a90a007b2025-11-11WarningsExact identifier
unii: ND2M416302
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
rxcui: 1737757
rxcui: 1737566
rxcui: 1737568
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
Sensorcaine MPFBUPIVACAINE HYDROCHLORIDEHenry Schein, Inc.78c6789d-773e-4b26-90bd-34a6b6d730ce2025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7TQO7W3VT8
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
SensorcaineBUPIVACAINE HYDROCHLORIDEHenry Schein, Inc.100201ad-6e4d-4e91-8b5c-621d0bf0dcc22025-11-07Warnings, Adverse reactionsExact identifier
unii: 7TQO7W3VT8
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

Reported adverse events (FAERS/openFDA)#

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