Home NDC 50844-392-24 NDC 50844-392-24 - 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 50844-392
Requested NDC 50844-392-24
Package NDCs from labels 50844-392-24, 50844-392-50, 50844-392-02, 50844-392-08, 50844-392-15, 50844-392-12, 50844-392-14, 50844-392-16
Manufacturer L.N.K. International, Inc. | LNK International, Inc.
Effective date 2026-06-18
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 44-392 L.N.K. International, Inc. | LNK International, Inc. 2026-06-18 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50844-392-02 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 13 50844-392-02 Ibuprofen 12 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 12 13 50844-392-08 Ibuprofen 24 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 24 13 50844-392-08 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 13 50844-392-12 Ibuprofen 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 13 50844-392-12 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 13 50844-392-14 Ibuprofen 500 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 500 13 50844-392-15 Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 13 50844-392-15 Ibuprofen 50 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 50 13 50844-392-16 Ibuprofen 1000 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 1000 13 50844-392-24 Ibuprofen 2 in 1 POUCH TABLET, FILM COATED 2 13 50844-392-50 Ibuprofen 50 in 1 CARTON TABLET, FILM COATED 50 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-392 IBUPROFEN TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 12 Current NDC, Legacy NDC, 12 package rows 20240628_027ded51-aa01-6619-3938-c8162a421cf3.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Ibuprofen ACTIVE INGREDIENT WK2XYI10QM IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Ibuprofen ACTIVE MOIETY WK2XYI10QM IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Carnauba Wax INACTIVE INGREDIENT R12CBM0EIZ IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Fd&c Yellow No. 6 INACTIVE INGREDIENT H77VEI93A8 IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Hypromellose INACTIVE INGREDIENT 3NXW29V3WO IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Lactose INACTIVE INGREDIENT J2B2A4N98G IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Magnesium Stearate INACTIVE INGREDIENT 70097M6I30 IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Polydextrose INACTIVE INGREDIENT VH2XOU12IE IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Polyethylene Glycol INACTIVE INGREDIENT 3WJQ0SDW1A IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Starch, Corn INACTIVE INGREDIENT O8232NY3SJ IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Stearic Acid INACTIVE INGREDIENT 4ELV7Z65AP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1 Titanium Dioxide INACTIVE INGREDIENT 15FIX9V2JP IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [L.N.K. INTERNATIONAL, INC.] 1
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 190 · 3,781 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen IBUPROFEN Shield Pharmaceuticals Corp 216e5600-56b4-44b0-88b7-69adfb245802 2026-08-06 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM 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 application number: ANDA075139 rxcui: 310965 unii: WK2XYI10QM Dye Free Ibuprofen IBUPROFEN Walgreen Company d3d093f9-207a-40d4-a7be-c6b5a544a0a7 2026-08-06 Warnings Exact identifier application number: ANDA075139 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 rxcui: 310965 unii: WK2XYI10QM Dye Free Ibuprofen IBUPROFEN Walgreen Company 8944a0e8-2928-4494-915f-d1e0a6d4bf5c 2026-08-04 Warnings Exact identifier application number: ANDA075139 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 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 EltaMD UV Active ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN CP Skin Health Group, Inc 39d16479-d491-4c19-aa11-674461687c7b 2026-08-03 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN NUVICARE LLC 7905edc1-2a45-4adc-a7bc-42b1ddb6ba59 2026-08-03 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen and famotidine IBUPROFEN AND FAMOTIDINE Doc Rx 9f5de6af-e555-4efd-a3ed-b72c34c051b6 2026-08-01 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM Ibuprofen and Pseudoephedrine Hydrochloride IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE Rite-Aid 483c3bb7-529e-4684-80e1-6646b050988e 2026-07-31 Warnings Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.