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 42 of 189 · 3,762 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Intellishade TruPhysical Clear SPF 50 TITANIUM DIOXIDE, ZINC OXIDE Revision, LLC 1305fa94-47d5-7a42-e063-6394a90a0aba 2026-01-13 Warnings Exact identifier unii: 15FIX9V2JP Intellishade Matte SPF 45 OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE Revision, LLC e213ae87-4db2-3070-e053-2995a90a083b 2026-01-13 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN L.N.K. International, Inc. 8ebe3e16-b7ae-d333-6671-5bc935e25900 2026-01-13 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM ibuprofen IBUPROFEN HyVee Inc 2fd51545-1d1f-4b2e-a084-d28ba223e720 2026-01-13 Warnings Exact identifier unii: WK2XYI10QM ibuprofen infants IBUPROFEN HyVee Inc e8fcaf17-234a-4d64-b621-9ca505884b0a 2026-01-12 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN L.N.K. International, Inc. d3b8d35a-10b5-a31c-8ced-eeb100c0fd7c 2026-01-12 Warnings Exact identifier application number: ANDA075010 rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Meijer Distribution Inc c0c64ba5-b6b0-4221-9e44-110d92c93782 2026-01-12 Warnings Exact identifier application number: ANDA075010 rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Coupler LLC 4831785a-cde2-79a2-e063-6294a90a9a40 2026-01-12 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM Blue Lizard Sensitive SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 9d20b230-2cce-4d90-e053-2995a90a4c03 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sheer SPF 50 Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Crown Laboratories c20fce25-8120-fe5d-e053-2a95a90a53a0 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sheer Face SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories baed8202-21fd-3a43-e053-2a95a90ada32 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sensitive Face Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Crown Laboratories 88dbd396-8955-271e-e053-2995a90a0a7a 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Baby SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 9d237fb7-4f5f-521d-e053-2a95a90a9734 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sensitive Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 1e4d49f4-9e77-48b5-bce5-ff04ed885a0f 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Baby SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 32d6e04a-fa30-ba48-e063-6394a90a1bbf 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Kids SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 2f780daa-4c91-5a68-e063-6394a90afd41 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sport SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 2f3844d8-0367-aad9-e063-6294a90a1fce 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Blue Lizard Sheer Face SPF 50 Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE Crown Laboratories 30cd79da-2f25-a42a-e063-6394a90a8332 2026-01-12 Warnings Exact identifier unii: 15FIX9V2JP Acetaminophen and Ibuprofen ACETAMINOPHEN AND IBUPROFEN BIONPHARMA INC. 4834aa7f-cb0c-ec58-e063-6394a90ae2fc 2026-01-12 Warnings Exact identifier unii: WK2XYI10QM Constipation Relief ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE Homeocare Laboratories 62374240-cd14-44e2-9405-5f8996faf047 2026-01-12 Warnings Exact identifier unii: ETJ7Z6XBU4
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.