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 39 of 67 · 1,339 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERHenry Schein, Inc.88403fcf-a276-42c0-88b6-bd84a720b5642025-05-29Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Diclofenac Sodium Delayed ReleaseDICLOFENAC SODIUMCarlsbad Technology, Inc.40879600-ba6c-43a8-aa5d-d0d41503d5932025-05-28Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
ALCOHOL PREP PADS MEDIUM STERILEISOPROPYL ALCOHOL CLOTHHUZHOU JUNDA INDUSTRY CO., LTD.361dcd60-c194-4c8b-e063-6294a90a425b2025-05-27WarningsExact identifier
unii: ND2M416302
HCS Alcohol Prep Pad LargeISOPROPYL ALCOHOLConcordance Healthcare Solutions, LLC.2cbe0c4c-440d-4f6c-88e8-363d3c798fba2025-05-27WarningsExact identifier
unii: ND2M416302
VLITEPRO First Aid WipesISOPROPYL ALCOHOL CLOTHYiwu Ori-Power Medtech Co., Ltd.35a7873a-e340-aae3-e063-6294a90a767f2025-05-26WarningsExact identifier
unii: ND2M416302
Mineral OilMINERAL OILATLANTIC BIOLOGICALS CORP.960502ae-2468-406e-8799-cacb01f2727e2025-05-23WarningsExact identifier
unii: T5L8T28FGP
XiclofenDICLOFENAC SODIUM, METHYL SALICYLATESTRAND HEALTH GROUP2d92d378-2e9c-f9d5-e063-6294a90ac7152025-05-21WarningsExact identifier
unii: QTG126297Q
Isopropyl AlcoholISOPROPYL ALCOHOLSafeway, Inc.29e5c152-15d7-4080-abf0-f76f8e9cbf5a2025-05-16WarningsExact identifier
unii: ND2M416302
Isopropyl Alcohol WintergreenISOPROPYL ALCOHOLSafeway, Inc.14a22d1e-e498-4661-ab30-6696b8b914d72025-05-16WarningsExact identifier
unii: ND2M416302
Isopropyl alcoholISOPROPYL ALCOHOLSafeway, Inc.69295fa8-0f0f-495c-a2ef-1414c6fa93a42025-05-16WarningsExact identifier
unii: ND2M416302
Eyesaline Emergency EyewashSTERILE EYESALINE EYEWASHHoneywell Safety Products USA, Inc.2d567518-4c54-7448-e063-6294a90a3e642025-05-14WarningsExact identifier
unii: 059QF0KO0R
DICLOFENAC SODIUMDICLOFENAC SODIUMAurobindo Pharma Limited3487033c-7c62-4034-8718-73a7c49b26a02025-05-09Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
Maokang Alcohol Prep Pad Saturated with 70% Isopropyl AlcoholISOPROPYL ALCOHOLChangzhou Maokang Medical Products Co., Ltda13a971c-769a-4909-8980-9e8bec4a03612025-05-09WarningsExact identifier
unii: ND2M416302
Diclofenac SodiumDICLOFENAC SODIUMPD-Rx Pharmaceuticals, Inc.87d5a720-f154-4c4b-b2d4-0ae58455dda02025-05-05Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
DiclonaLIDOCAINE 4.5%, DICLOFENAC 1%Advanced Rx of Tennessee, LLC34685ef2-0015-8941-e063-6294a90ad0f72025-05-05Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
DICLOFENAC SODIUMDICLOFENAC SODIUM TOPICAL GEL, 1%Dr. Reddy's Laboratories Inc.03abebd6-426a-9d05-3dff-1964773894302025-05-05WarningsExact identifier
application number: ANDA210986
rxcui: 855633
unii: QTG126297Q
Diclofenac sodiumDICLOFENAC SODIUMBluePoint Laboratories896e3f7d-88e6-4563-b879-a2757d19fd622025-05-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
ALCOHOL PREP PADS LARGE STERILEISOPROPYL ALCOHOL CLOTHHUZHOU JUNDA INDUSTRY CO., LTD.367ab42b-46fe-90f7-e063-6394a90ad2032025-05-01WarningsExact identifier
unii: ND2M416302
DICLOFENAC SODIUMDICLOFENAC SODIUMAdvagen Pharma Ltd72419a68-4c9d-44e0-9b43-922440e2c8d72025-04-30Warnings, Adverse reactionsExact identifier
unii: QTG126297Q
ANTYZE Smelling SaltsSMELLING SALTSShenzhen Nanjun Technology Co., Ltd33e8773c-0bea-9640-e063-6394a90ae14b2025-04-29WarningsExact identifier
unii: 5138Q19F1X

Reported adverse events (FAERS/openFDA)#

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