Home NDC 50844-291-24 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 Label Manufacturer Effective date Type Quality Plus 44-291 L.N.K. International, Inc. | LNK International, Inc. 2026-06-09 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50844-291-01 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-01 Ibuprofen 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 21 50844-291-02 Ibuprofen 12 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 12 21 50844-291-02 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-03 Ibuprofen 10 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 10 21 50844-291-08 Ibuprofen 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 21 50844-291-08 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-10 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-10 Ibuprofen 40 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 40 21 50844-291-11 Ibuprofen 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 21 50844-291-11 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-12 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-12 Ibuprofen 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 21 50844-291-13 Ibuprofen 250 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 250 21 50844-291-13 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-14 Ibuprofen 500 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 500 21 50844-291-15 Ibuprofen 50 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 50 21 50844-291-15 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-16 Ibuprofen 1000 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 1000 21 50844-291-17 Ibuprofen 300 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 300 21 50844-291-24 Ibuprofen 2 in 1 POUCH TABLET, FILM COATED 2 21 50844-291-29 Ibuprofen 150 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 150 21 50844-291-29 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 21 50844-291-50 Ibuprofen 50 in 1 CARTON TABLET, FILM COATED 50 21 50844-291-99 Ibuprofen 250 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 250 21
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-291 IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 20 Current NDC, Legacy NDC, 25 package rows 20240628_57b39311-bc20-ace6-75a9-a07a9311b373.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded IBUPROFEN ACTIVE INGREDIENT WK2XYI10QM IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 IBUPROFEN ACTIVE MOIETY WK2XYI10QM IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 3 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP IBUPROFEN 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 5 of 192 · 3,834 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Journee Firm Riche Broad Spectrum Sunscreen SPF 30 TITANIUM DIOXIDE AND ZINC OXIDE Merz North America, Inc. d4d4bfcf-3674-4847-8ad8-1716a8e821ae 2026-08-10 Warnings Exact identifier unii: 15FIX9V2JP VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen TITANIUM DIOXIDE, OCTINOXATE LCM TECHNOLOGY Co., Ltd 4cbbf8aa-8910-b7e7-e063-6294a90a4f07 2026-08-07 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen minis IBUPROFEN Walgreens 6d1d131d-0741-4a75-8383-9322f4f3faab 2026-08-06 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Shield Pharmaceuticals Corp 216e5600-56b4-44b0-88b7-69adfb245802 2026-08-06 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Calamine FERRIC OXIDE RED The Kroger Co. 9ddcd6ba-1aed-48f8-a91a-54bd6f0d9308 2026-08-06 Warnings, Adverse reactions Exact identifier unii: 1K09F3G675 EltaMD UV Restore TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN CP Skin Health Group, Inc 37fee381-ce6b-4949-9a4a-778aa839fb84 2026-08-06 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN COSTCO WHOLESALE CORPORATION 4b8ad98e-de76-4f49-3b89-01e9dd5cde16 2026-08-06 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Dye Free Ibuprofen IBUPROFEN Walgreen Company d3d093f9-207a-40d4-a7be-c6b5a544a0a7 2026-08-06 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN P & L Development, LLC 159b68b7-54e5-4f83-b632-f49e7b4b14a5 2026-08-05 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Walgreen Company c118b290-f821-4e73-906e-8a93edaf34e4 2026-08-05 Warnings Exact identifier application number: ANDA075010 rxcui: 310965 unii: WK2XYI10QM Dye Free Ibuprofen IBUPROFEN Walgreen Company 8944a0e8-2928-4494-915f-d1e0a6d4bf5c 2026-08-04 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM ROROBELL WAWA Whitening Tooth SILICA, HYDROGEN PEROXIDE, TOCOPHERYL ACETATE ROROBELL 58336a0d-49dd-ef13-e063-6394a90a38c1 2026-08-04 Warnings Exact identifier unii: ETJ7Z6XBU4 Ibuprofen IBUPROFEN REMEDYREPACK INC. 560e4e05-21e0-4b2a-ab2f-872b5dbb3901 2026-08-04 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM SurviveX Travel Med MOD CONVENIENCE KIT Intent Brands LLC 522da86b-cfd7-dd20-e063-6394a90a51c6 2026-08-04 Warnings Exact identifier rxcui: 310965 Silicea 6X SILICON DIOXIDE Hyland's Inc. db4be3c1-aa7e-24a2-e053-2a95a90a0c66 2026-08-04 Warnings Exact identifier unii: ETJ7Z6XBU4 Ibuprofen IBUPROFEN Chain Drug Marketing Association, Inc. 733d0b21-c177-4c60-9243-2f1e7cb5854a 2026-08-04 Warnings Exact identifier application number: ANDA075010 rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Pioneer Life Sciences, LLC 8abd74a4-ad33-4c10-b677-acb469f815e6 2026-08-03 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Pioneer Life Sciences, LLC 291602fa-8ebe-4200-bba7-9798c90f8a50 2026-08-03 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8% Lale Cosmetics LLC 581fb0cd-c55d-d562-e063-6394a90a7f11 2026-08-03 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN NUVICARE LLC b063d2dc-d579-46e7-8cfc-1596c803c7f9 2026-08-03 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.