FDA.reportPublic FDA data

NDC 51688-6009 - A3736-22

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
51688-6009
Package NDCs from labels
51688-6009-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.
Effective date
2011-06-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
A3736-22 - Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.2011-06-03MEDICAL DEVICE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-4713-65A3736-225 mL in 1 AMPULEINJECTION, SOLUTION5 mL10 mg in 1mL4
51688-6009-2A3736-221 in 1 PACKAGE, COMBINATIONKIT14
51688-6009-2A3736-2210 in 1 CASEKIT104
52380-0001-3A3736-229.8 g in 1 PACKETSOLUTION9.8 g9.8 g in 100g4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51688-6009(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]44 package rows20110607_c38ce5e9-5b1c-4ec8-bf85-12199a84f5a5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENTEC2CNF7XFP(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99M(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
IODINEACTIVE MOIETY9679TC07X4(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
LidocaineACTIVE MOIETY98PI200987(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CB(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9T(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8X(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32I(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA74(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4
WaterINACTIVE INGREDIENT059QF0KO0R(REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.]4

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 24 of 71 · 1,417 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Easy Care First Aid EyewashWATERTender Corporationa070aac8-e6d2-ef10-e053-2a95a90aa5b12025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.e07a064b-f680-405c-bbcd-24fac430951e2025-11-24WarningsExact identifier
unii: 059QF0KO0R
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Natural Eyes Floaters ReliefCHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEATRP Company445dc831-195e-4b25-e063-6294a90a6efd2025-11-24WarningsExact identifier
unii: 451W47IQ8X
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Vital Female Sexual EnergyAGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, ONOSMODIUM VIRGINIANUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SEPIA, THUJA OCCIDENTALISLiddell Laboratories, Inc.1ca43c82-62b0-4191-81a4-27f7f94109dd2025-11-20WarningsExact identifier
unii: 451W47IQ8X
Sodium ChlorideSODIUM CHLORIDEWalgreen Companyd112a344-33cc-41d3-bae6-492631ebdba72025-11-19WarningsExact identifier
unii: 451W47IQ8X
PVP-Iodine Swabstick ThreesPOVIDONE-IODINEDukal LLC5af20b49-11b1-4b15-bb7f-eccda2c469972025-11-19WarningsExact identifier
unii: 85H0HZU99M
PVP-I Pouch foil-foilPOVIDONE-IODINEDukal LLC45aefabf-5283-411a-b509-7499776359382025-11-19WarningsExact identifier
rxcui: 312564
unii: 85H0HZU99M
PVP-I Prep Pads foil-foilPOVIDONE-IODINEDukal LLC95c35c0d-bebb-46d0-8e97-f3d2541723ad2025-11-19WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine GelPOVIDONE-IODINEDukal LLC2bebe082-59b6-17c1-e063-6294a90a9a522025-11-19WarningsExact identifier
unii: 85H0HZU99M
Povidone-Iodine Gel SwabstickPOVIDONE IODINEDukal LLC98be29e6-0c9b-22a6-e053-2995a90a9f8c2025-11-19WarningsExact identifier
unii: 85H0HZU99M
Dukal Povidone-Iodine Scrub Winged SpongesPOVIDONE-IODINE SCRUB WINGED SPONGESDukal LLCe8bce905-929e-30e4-e053-2a95a90a909f2025-11-19WarningsExact identifier
unii: 85H0HZU99M
Dukal Povidone-Iodine Paint Sponge StickPOVIDONE-IODINE PAINT SPONGE STICKDukal LLCf1dc2bc6-f459-af82-e053-2995a90afbd72025-11-19WarningsExact identifier
unii: 85H0HZU99M
PVP-I Prep Pads paper-foilPOVIDONE-IODINEDukal LLCf4596b0c-0e04-d71a-e053-2995a90a3b202025-11-19WarningsExact identifier
unii: 85H0HZU99M
Dukal Povidone-Iodine Scrub Sponge SticksPOVIDONE-IODINE SCRUB SPONGE STICKSDukal LLCf6f5dc9a-b578-70c1-e053-6394a90acdb02025-11-19WarningsExact identifier
unii: 85H0HZU99M
Sodium chlorideSODIUM CHLORIDEFresenius Kabi USA, LLCce0c8c6f-734a-400f-9b60-a3b1e263f25f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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