FDA.reportPublic FDA data

NDC 50844-291-24 - 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
50844-291
Requested NDC
50844-291-24
Package NDCs from labels
50844-291-24, 50844-291-50, 50844-291-03, 50844-291-02, 50844-291-08, 50844-291-01, 50844-291-10, 50844-291-15, 50844-291-11, 50844-291-12, 50844-291-29, 50844-291-99, 50844-291-13, 50844-291-17, 50844-291-14, 50844-291-16
Manufacturer
L.N.K. International, Inc. | LNK International, Inc.
Effective date
2026-06-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Quality Plus 44-291L.N.K. International, Inc. | LNK International, Inc.2026-06-09HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50844-291-01Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-01Ibuprofen30 in 1 BOTTLE, PLASTICTABLET, FILM COATED3021
50844-291-02Ibuprofen12 in 1 BOTTLE, PLASTICTABLET, FILM COATED1221
50844-291-02Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-03Ibuprofen10 in 1 BOTTLE, PLASTICTABLET, FILM COATED1021
50844-291-08Ibuprofen24 in 1 BOTTLE, PLASTICTABLET, FILM COATED2421
50844-291-08Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-10Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-10Ibuprofen40 in 1 BOTTLE, PLASTICTABLET, FILM COATED4021
50844-291-11Ibuprofen60 in 1 BOTTLE, PLASTICTABLET, FILM COATED6021
50844-291-11Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-12Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-12Ibuprofen100 in 1 BOTTLE, PLASTICTABLET, FILM COATED10021
50844-291-13Ibuprofen250 in 1 BOTTLE, PLASTICTABLET, FILM COATED25021
50844-291-13Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-14Ibuprofen500 in 1 BOTTLE, PLASTICTABLET, FILM COATED50021
50844-291-15Ibuprofen50 in 1 BOTTLE, PLASTICTABLET, FILM COATED5021
50844-291-15Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-16Ibuprofen1000 in 1 BOTTLE, PLASTICTABLET, FILM COATED100021
50844-291-17Ibuprofen300 in 1 BOTTLE, PLASTICTABLET, FILM COATED30021
50844-291-24Ibuprofen2 in 1 POUCHTABLET, FILM COATED221
50844-291-29Ibuprofen150 in 1 BOTTLE, PLASTICTABLET, FILM COATED15021
50844-291-29Ibuprofen1 in 1 CARTONTABLET, FILM COATED121
50844-291-50Ibuprofen50 in 1 CARTONTABLET, FILM COATED5021
50844-291-99Ibuprofen250 in 1 BOTTLE, PLASTICTABLET, FILM COATED25021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50844-291IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]20Current NDC, Legacy NDC, 25 package rows20240628_57b39311-bc20-ace6-75a9-a07a9311b373.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IBUPROFENACTIVE INGREDIENTWK2XYI10QMIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
IBUPROFENACTIVE MOIETYWK2XYI10QMIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IEIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPIBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.]3

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 34 of 190 · 3,781 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CareOne IbuprofenIBUPROFENAmerican Sales Company03cdff8a-8890-440d-82b5-54ce809f88cc2026-02-03WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
Pain Relief IbuprofenIBUPROFENRite Aid Corporationc85c3d1f-7639-4cfa-bf3a-424b61757b1a2026-02-03WarningsExact identifier
application number: ANDA075010
rxcui: 310965
unii: WK2XYI10QM
Motrin Dual Action With TylenolACETAMINOPHEN AND IBUPROFENKenvue Brands LLCf2ee9cf5-02b7-6612-e053-2995a90a90c42026-02-03WarningsExact identifier
unii: WK2XYI10QM
Meteoric Iron PrunusMETEORIC IRON PRUNUSUriel Pharmacy Inc.e9020757-2393-4a22-9665-25da0a0993d02026-02-03WarningsExact identifier
unii: ETJ7Z6XBU4
Mold, Yeast and DustACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEANaturalCaree0f53f47-acd9-43e2-a7a2-2a500bc9dc1b2026-02-03WarningsExact identifier
unii: ETJ7Z6XBU4
ibuprofenIBUPROFENHyVee Inc5233c409-3743-4312-9f75-14ded6755b5c2026-02-02WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
Dr.Oracle AIR FIT DEFENSE SOOTHING SUNSCREENHOMOSALATE, OCTYL SALICYLATE, TITANIUM DIOXIDE, ZINC OXIDEOracle Cosmetic Co., Ltd.21424f78-f8d5-6a9b-e063-6294a90ab7dc2026-02-02WarningsExact identifier
unii: 15FIX9V2JP
Aquavit 1AQUAVIT 1Uriel Pharmacy Inc.2354fcfc-05a2-444a-ace4-b3df614131572026-02-02WarningsExact identifier
unii: 1K09F3G675
pain relief ibuprofenIBUPROFENRite Aid Corporation2bd1438e-27b1-81ff-f8e1-0f5b50b045812026-02-02WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
IbuprofenIBUPROFENL.N.K. International, Inc.8b5eec38-bdf3-4f27-802f-f4c732ae5c7d2026-02-02WarningsExact identifier
unii: WK2XYI10QM
IbuprofenIBUPROFENH E B88c7486b-f9a7-4856-a25a-7c06e1382f1a2026-02-02WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
Reef safe unscented SPF 50 mineral sunscreen 01TITANIUM DIOXIDE, ZINC OXIDECosmuses Cosmetics (Ningbo) Co., Ltd.49a77ad4-508c-9617-e063-6394a90a56232026-01-30WarningsExact identifier
unii: 15FIX9V2JP
JOSIE MARAN ARGAN SUN MILK MINERAL SUNSCREEN BROAD SPECTRUM SPF 33TITANIUM DIOXIDE AND ZINC OXIDECosmetic Solutions LLCd65ae1c9-dff5-4612-b8be-fa59bba03b812026-01-30WarningsExact identifier
unii: 15FIX9V2JP
IbuprofenIBUPROFENStrategic Sourcing Services, LLCdc469eb2-89cc-46c9-9304-f6cf119c05702026-01-29WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
CalamineCALAMINEAMERISOURCE BERGEN90d9d908-57ea-4062-ade0-8a4888939c912026-01-29Warnings, Adverse reactionsExact identifier
unii: 1K09F3G675
CaldolorIBUPROFENCumberland Pharmaceuticals Inc.1eaa7790-f1a1-4f51-b10a-cbbaf033f6842026-01-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WK2XYI10QM
SHISEIDO SPORTS BB DARKOCTINOXATE AND TITANIUM DIOXIDESHISEIDO AMERICAS CORPORATIONf4fc4b6a-9507-496e-9ecb-8400055ecf2d2026-01-28WarningsExact identifier
unii: 15FIX9V2JP
Hampton Sun SPF 30 MineralZINC OXIDE 7.20% TITANIUM DIOXIDE 4.00%S&C Hampton Sun LLCb8ee428e-07d3-4c6c-853c-cfbe3e4002d92026-01-28WarningsExact identifier
unii: 15FIX9V2JP
IBUPROFEN 200 MGIBUPROFEN 200 MGFarmacias De Similares TX LLC441f7920-5666-5a3e-e063-6294a90a55832026-01-28WarningsExact identifier
rxcui: 310965
unii: WK2XYI10QM
IbuprofenIBUPROFENSoftgel Healthcare Private Limited2b07ace6-6766-0a06-e063-6294a90ad1bd2026-01-27WarningsExact identifier
unii: WK2XYI10QM

Reported adverse events (FAERS/openFDA)#

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