FDA.reportPublic FDA data

NDC 50090-5446-07 - Ibuprofen

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
50090-5446
Requested NDC
50090-5446-07
Package NDCs from labels
50090-5446-8, 50090-5446-1, 50090-5446-4, 50090-5446-9, 50090-5446-7, 50090-5446-0, 50090-5446-5, 50090-5446-2, 50090-5446-3, 50090-5446-07
Manufacturer
A-S Medication Solutions
Effective date
2025-12-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ibuprofen - A-S Medication SolutionsA-S Medication Solutions2025-12-18Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-5446-0Ibuprofen10 in 1 BOTTLETABLET1016
50090-5446-1Ibuprofen15 in 1 BOTTLETABLET1516
50090-5446-2Ibuprofen30 in 1 BOTTLETABLET3016
50090-5446-3Ibuprofen45 in 1 BOTTLETABLET4516
50090-5446-4Ibuprofen60 in 1 BOTTLETABLET6016
50090-5446-5Ibuprofen100 in 1 BOTTLETABLET10016
50090-5446-7Ibuprofen21 in 1 BOTTLETABLET2116
50090-5446-8Ibuprofen12 in 1 BOTTLETABLET1216
50090-5446-9Ibuprofen40 in 1 BOTTLETABLET4016

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-5446IBUPROFEN TABLET [A-S MEDICATION SOLUTIONS]14Current NDC, Legacy NDC, 9 package rows20240530_f24582be-8d70-4848-bd54-e55fa28f394f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-5446-0EA - Each50090-5446a7773238-2ab2-4e57-85c6-16d42422f1ad12024-06-10
50090-5446-1EA - Each50090-54464699bffd-8c17-4951-be12-b4ba0864e33812024-06-10
50090-5446-2EA - Each50090-5446c25a556a-f3a7-4a87-ade9-73e78cda68fb12024-03-12
50090-5446-3EA - Each50090-544674836018-6b93-4a5a-947a-c6b3124d14c512024-06-10
50090-5446-4EA - Each50090-544691ee36be-422f-49d7-8993-b7989628de5412024-06-10
50090-5446-5EA - Each50090-5446e1f5a3f9-e4c8-4dd9-b8a1-20ce58a008c412024-06-10
50090-5446-7EA - Each50090-5446cf2dffee-09ea-4c41-ab6f-eb460525c6eb12024-06-10
50090-5446-8EA - Each50090-544607fff2af-f163-43d0-b9dc-505bdb000daf12024-06-10
50090-5446-9EA - Each50090-54469fcf22a4-f0cb-40c7-b9c6-a45b13f2026612024-06-10

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 52 of 192 · 3,827 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Family Wellness Artificial TearsPOLYVINYL ALCOHOL, POVIDONEFamily Dollar Services, Inc.facd329b-1923-61df-e053-6294a90ab7382025-12-30WarningsExact identifier
unii: 532B59J990
Artificial TearsPOLYVINYL ALCOHOL, POVIDONEKC Pharmaceuticals, Inc.eb6eb6c4-1609-407b-84e4-c7509811f3c02025-12-30WarningsExact identifier
unii: 532B59J990
Publix Artificial Tears Eye DropsPOLYVINYL ALCOHOL, POVIDONEPublix Super Markets, Inc.f5d1394b-0fe8-c372-e053-2a95a90a1f782025-12-30WarningsExact identifier
unii: 532B59J990
Best Choice Artificial TearsPOLYVINYL ALCOHOL, POVIDONEBest Choicef5ba63f3-7966-81fe-e053-2995a90a342c2025-12-30WarningsExact identifier
unii: 532B59J990
Kroger Eye Drops Artificial TearsPOLYVINYL ALCOHOL, POVIDONEThe Kroger Companyf76f08c5-0111-8bc5-e053-6294a90a16ee2025-12-30WarningsExact identifier
unii: 532B59J990
CareOne Artificial Tears Eye Drops 15mLPOLYVINYL ALCOHOL, POVIDONERetail Business Services, LLC92fded6b-91fd-d82e-e053-2a95a90ab5232025-12-30WarningsExact identifier
unii: 532B59J990
Quality Choice Artificial Tears Lubricant Eye DropsPOLYVINYL ALCOHOL, POVIDONEChain Drug Marketing Association, Inc.1f669655-4bc7-0175-e063-6294a90a305a2025-12-30WarningsExact identifier
unii: 532B59J990
Equate Artificial TearsPOLYVINYL ALCOHOL, POVIDONEWalmart, Inc.ead9f271-0f15-1fff-e053-2a95a90a93ac2025-12-30WarningsExact identifier
unii: 532B59J990
IBUPROFENIBUPROFENTIME CAP LABORATORIES, INCe0a8315a-80a5-4be3-aad1-3d01f00df4942025-12-29WarningsExact identifier
unii: WK2XYI10QM
SPF 30 SunscreenZINC OXIDE, TITANIUM DIOXIDECLEUREf5512f34-08ee-b0f6-e053-2a95a90ab5bd2025-12-29WarningsExact identifier
unii: 15FIX9V2JP
RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20OCTINOXATE AND TITANIUM DIOXIDEESTEE LAUDER INC897b8edb-f089-4a49-baca-e05806b0a0682025-12-29WarningsExact identifier
unii: 15FIX9V2JP
OI LIN SUNMILK SUNSCREEN SPF 30SUNSCREEN, TITANIUM DIOXIDESunrider Manufacturing L.P.26b57314-1616-4ca4-b65f-a363c525b4322025-12-29WarningsExact identifier
unii: 15FIX9V2JP
Childrens Ibuprofen Oral Suspension Original Berry FlavorIBUPROFENPuro Pharma Inc.6b993b25-9c81-4d75-b332-6de3f6c3b4c92025-12-27WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENSun Pharmaceutical Industries, Inc.a8b46ae5-67bc-494d-850e-b4e4ed5a33b32025-12-27Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENNorthwind Health Company, LLCf2a08223-a73a-5461-e053-2995a90a3bce2025-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197806
unii: WK2XYI10QM
IbuprofenIBUPROFENNorthwind Health Company, LLCab074ae8-5696-5327-e053-2a95a90a7ce32025-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 197805
unii: WK2XYI10QM
Childrens Ibuprofen Oral SuspensionIBUPROFENAptaPharma Inc.40936019-74ab-4b25-a502-7bbc6e12034a2025-12-26WarningsExact identifier
unii: WK2XYI10QM
Childrens Ibuprofen GrapeIBUPROFENAptaPharma Inc.7caca7e2-6652-45fc-9538-275b43a1594e2025-12-26WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENHumanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd46a9424c-fd7d-f88b-e063-6294a90abceb2025-12-24WarningsExact identifier
unii: WK2XYI10QM
StellaLife VEGA Oral CareSPRAYStellaLife, Inc.b8ba495e-2cfe-092c-e053-2995a90a3fd32025-12-24WarningsExact identifier
unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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