FDA.reportPublic FDA data

NDC 68071-2239-01 - Diclofenac Sodium

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
68071-2239
Requested NDC
68071-2239-01
Package NDCs from labels
68071-2239-1, 68071-2239-01
Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2025-01-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Diclofenac Sodium - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2025-01-02HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-2239-12022-02-07C16284748780-1d6a99b39-fa3c-a426-e053-dadaa90af4c2These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL GEL safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL GEL. DICLOFENAC SODIUM topical gel, 1% for topical use only Initial U.S. Approval: 1988
68071-2239-12022-01-28C16284748780-1d6a99b39-fa3c-a426-e053-dadaa90af4c2These highlights do not include all the information needed to use DICLOFENAC SODIUM TOPICAL GEL safely and effectively. See full prescribing information for DICLOFENAC SODIUM TOPICAL GEL. DICLOFENAC SODIUM topical gel, 1% for topical use only Initial U.S. Approval: 1988

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-2239-1Diclofenac Sodium100 g in 1 TUBEGEL1004
68071-2239-1Diclofenac Sodium1 in 1 CARTONGEL14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-2239DICLOFENAC SODIUM GEL [NUCARE PHARMACEUTICALS,INC.]4Current NDC, Legacy NDC, 2 package rows20250104_ad193f94-f8d0-8482-e053-2995a90a35a4.zip

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 33 of 67 · 1,339 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ProCure Alcohol Prep PadsISOPROPYL ALCOHOL 70%Twin Med LLC3f6816c2-a0eb-36d7-e063-6294a90a823b2025-09-30WarningsExact identifier
unii: ND2M416302
ProCure Alcohol Prep PadsISOPROPYL ALCOHOL 70%Twin Med LLC87ae4b97-dbe9-4827-905d-4abf42df011e2025-09-30WarningsExact identifier
unii: ND2M416302
Xpect EyewashEYEWASHCintas Corporation1d69365d-662b-4248-8fa9-1629451b549a2025-09-30WarningsExact identifier
unii: 059QF0KO0R
EVR Alcohol Prep PadsISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltd.3ffba233-6106-f633-e063-6394a90a96fe2025-09-29WarningsExact identifier
unii: ND2M416302
ProHeal Alcohol Prep PadISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltd.3ffc0619-eb13-77af-e063-6394a90a2fd92025-09-29WarningsExact identifier
unii: ND2M416302
First Aid Direct Alcohol WipeISOPROPYL ALCOHOLCintas Corporation6a71449e-9a97-4923-8ec1-b1deb45b57462025-09-29WarningsExact identifier
unii: ND2M416302
Leader Ready to Use Mineral Oil LaxativeMINERAL OILCardinal Healthb8494d02-8a7d-47b4-80b0-b8ab51b625fd2025-09-29WarningsExact identifier
unii: T5L8T28FGP
ARTHRITIS PAIN RELIEVINGDICLOFENAC SODIUMWalgreen Companyb1850a16-54f1-4210-abdf-26414da8b3d92025-09-29WarningsExact identifier
rxcui: 855633
unii: QTG126297Q
Xpect Alcohol WipesALCOHOL WIPESCintas Corporation51185b9a-ed6b-4a49-b524-b3ff0d5c62902025-09-29WarningsExact identifier
unii: ND2M416302
FOSTER AND THRIVE ARTHRITIS PAINDICLOFENAC SODIUMStrategic Sourcing Services LLCf9f4e55f-ffad-4df7-9b3c-1e7c3a3723c12025-09-27WarningsExact identifier
rxcui: 855633
unii: QTG126297Q
CheBoho TEA TREE ACNECHEBOHO TEA TREE ACNEOpalshi(Guangzhou)E-commerce Co. Ltd.3fc4cf84-b2da-c593-e063-6394a90abc5c2025-09-27WarningsExact identifier
unii: 059QF0KO0R
HUMCO 1 Percent IodineISOPROPYL ALCOHOLHumco Holding Group, Inc.139efeef-be20-4362-a5ba-158b8fa40e0d2025-09-22WarningsExact identifier
unii: ND2M416302
Xpect Isopropyl AlcoholISOPROPYL ALCOHOLCintas Corpb55fe473-45d2-48d3-b4d4-fc0993cb4dfe2025-09-22WarningsExact identifier
unii: ND2M416302
Sterile WaterWATERProPharma Distribution3f2ae880-852f-b45d-e063-6394a90aa1cc2025-09-19Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
DG HEALTH ARTHRITIS PAINDICLOFENAC SODIUMDolgencorp Inc6479e4bb-0790-483e-bfe3-a54d549aa5d22025-09-15WarningsExact identifier
rxcui: 855633
unii: QTG126297Q
Dry eye reliefPOLYETHYLENE GLYCOL AND PROPYLENE GLYCOLCARDINAL HEALTH 110, LLC. DBA LEADERf8da3af5-9172-4023-be82-0fd5bd8916162025-09-12WarningsExact identifier
unii: 6DC9Q167V3
Diclofenac Sodium and MisoprostolDICLOFENAC SODIUM AND MISOPROSTOLBluePoint Laboratories9a22cb4b-e49a-4bd7-b235-47405c3026582025-09-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
UpSniff Smelling SaltsSMELLING SALTSShenzhen Nanjun Technology Co., Ltd3e7e4c2c-08bc-37b7-e063-6394a90a6b212025-09-10WarningsExact identifier
unii: 5138Q19F1X
Diclolidol KitLIDOCAINE HCL, DICLOFENAC SODIUMPureTek Corporation3e63324b-e761-9367-e063-6394a90a29812025-09-09Warnings, Adverse reactionsExact identifier
rxcui: 855633
Medi-First First Aid Eye WashPURIFIED WATERUnifirst First Aid Corporationdcd7fe56-ff5c-4c8d-a415-6e363d7e53f42025-09-08WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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