FDA.reportPublic FDA data

NDC 51688-5232 - A3535 PORTEX PROCEDURAL

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
51688-5232
Package NDCs from labels
51688-5232-2
Manufacturer
Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.
Effective date
2016-06-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
LIDOCAINE - Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.Smiths Medical ASD, Inc. | Hospira, Inc. | Aplicare, Inc.2016-06-14MEDICAL DEVICE

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LIDOCAINE HYDROCHLORIDE ANHYDROUSACTIVE INGREDIENTEC2CNF7XFPA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99MA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
IODINEACTIVE MOIETY9679TC07X4A3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
LidocaineACTIVE MOIETY98PI200987A3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9TA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
Sodium HydroxideINACTIVE INGREDIENT55X04QC32IA3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA74A3535 PORTEX PROCEDURAL () KIT [SMITHS MEDICAL ASD, INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RA3535 PORTEX PROCEDURAL () 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 21 of 104 · 2,066 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Vital Female Sexual EnergyAGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SABAL SERRULATA, SEPIA, THUJA OCCIDENTALISLiddell Laboratories, Inc.7b15d6fa-eb04-41d2-8a01-6e7408ccf4d32026-01-30WarningsExact identifier
unii: 451W47IQ8X
Additive Formula 3DEXTROSE MONOHYDRATE, TRISODIUM CITRATE DIHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, CITRIC ACID MONOHYDRATE, AND ADENINETerumo BCT, Ltd9a5247a1-cc05-442d-b2d0-950f887f03c22026-01-30Warnings, Adverse reactionsExact identifier
unii: 2968PHW8QP
unii: 451W47IQ8X
CVS ULTRA FINE MOISTURIZING SALINE MISTNASAL MISTCVS44821c47-63f9-5d0a-e063-6394a90a555d2026-01-29WarningsExact identifier
unii: 451W47IQ8X
First Aid AntisepticFIRST AID ANTISEPTICAmerisource Bergen6719db46-a6e3-4f0a-828c-fe89a51879892026-01-29Warnings, Adverse reactionsExact identifier
unii: 85H0HZU99M
Equate Ready-to-Use Enema LaxativeSODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMWalMart04c7440e-5b25-4b63-9604-321298d510212026-01-29WarningsExact identifier
unii: GR686LBA74
Quality Choice LaxativeSODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMChain Drug Marketing Association1cac3b6b-155b-47bb-bb79-17c55d3457362026-01-28WarningsExact identifier
unii: GR686LBA74
VonaFlex Effective Pain Relief Topical AnalgesicLIDOCAINE HYDROCHLORIDEOPTIMAL LABORATORIES, LLC0901244a-7d41-413a-b424-92a807532f282026-01-28WarningsExact identifier
unii: V13007Z41A
ALOE ICE SUNBURN RELIEFLIDOCAINE HYDROCHLORIDEAloe Care International, LLC56866fa8-052e-497c-a954-978d7d6289492026-01-28WarningsExact identifier
unii: V13007Z41A
TRIDERMA PAIN RELIEFLIDOCAINE HCL, MENTHOLGenuine Virgin Aloe Corporation9172d6cd-f7d3-421e-a8b5-c1cb3325ada52026-01-27WarningsExact identifier
unii: V13007Z41A
Sodium ChlorideSODIUM CHLORIDENephron Pharmaceuticals Corporationa4edf2d5-a9ff-30d4-e053-2995a90a56502026-01-26Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
MedlinePOVIDONE-IODINEMedline Industries, LP48ebfdd6-d346-7e26-e063-6394a90af11a2026-01-23WarningsExact identifier
unii: 85H0HZU99M
EVERLIT SURVIVAL IODINE PREP PADSPOVIDONE-IODINEEVERLIT GLOBAL INC.3a03fc8d-2653-9183-e063-6294a90ad76e2026-01-23WarningsExact identifier
unii: 85H0HZU99M
CVS Health Maximum Strength Lidocaine Pain Relief Cream Plus MentholLIDOCAINE HCL, MENTHOLCVS Pharmacy8aaffa3f-f82f-470c-902d-f366f1a663052026-01-21WarningsExact identifier
unii: V13007Z41A
Lights Povindone Iodine SwabstickPOVIDONE-IODINELights Medical Manufacture Co., Ltd.977b6077-bf47-4e02-bde4-c752e73d76282026-01-21WarningsExact identifier
unii: 85H0HZU99M
Lights Povindone Iodine ScrubPOVIDONE-IODINELights Medical Manufacture Co., Ltd.000bf57b-1805-4746-bf1c-32856241213a2026-01-21WarningsExact identifier
unii: 85H0HZU99M
Lights Povidone Iodine SolutionPOVIDONE-IODINELights Medical Manufacture Co., Ltd.6946eb98-6870-4b21-9dda-b01a8adab84b2026-01-21WarningsExact identifier
unii: 85H0HZU99M
Lights Povidone Iodine Prep PadPOVIDONE-IODINELights Medical Manufacture Co., Ltd.e561332d-e419-43db-a68e-0c0d49b01c9a2026-01-21WarningsExact identifier
unii: 85H0HZU99M
Lights Povindone Iodine SwabstickPOVIDONE-IODINELights Medical Manufacture Co., Ltd.2610fde4-4572-4d15-a970-f6d3beb734fe2026-01-21WarningsExact identifier
unii: 85H0HZU99M
Lights Povidone Iodine SolutionPOVIDONE-IODINELights Medical Manufacture Co., Ltd.7d4a92be-0601-4256-bc5b-bc1b07d97bb72026-01-21WarningsExact identifier
unii: 85H0HZU99M
Betadine GarglePOVIDONE-IODINEAtlantis Consumer Healthcare, Inc.5f0a3377-1398-2603-c632-f0d214bb88ec2026-01-21WarningsExact identifier
unii: 85H0HZU99M

Reported adverse events (FAERS/openFDA)#

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