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 11 of 192 · 3,834 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Delicate Beige Perfecting Makeup Broad Spectrum SPF 25 OCTINOXATE, TITANIUM DIOXIDE Merle Norman Cosmetics, Inc 551928b4-74bb-3f6c-e063-6294a90a6b83 2026-06-25 Warnings Exact identifier unii: 15FIX9V2JP Alabaster Beige Perfecting Makeup Broad Spectrum SPF 25 OCTINOXATE, TITANIUM DIOXIDE Merle Norman Cosmetics, Inc 5519290c-b040-6a37-e063-6394a90a8a1d 2026-06-25 Warnings Exact identifier unii: 15FIX9V2JP Soft Bisque Perfecting Makeup Broad Spectrum SPF 25 OCTINOXATE, TITANIUM DIOXIDE Merle Norman Cosmetics, Inc 551ab7d1-dd2f-c6d8-e063-6394a90aff65 2026-06-25 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen Mini Dye Free IBUPROFEN CVS Pharmacy 42c7dbec-2e53-70ae-e063-6294a90a16e6 2026-06-25 Warnings Exact identifier unii: WK2XYI10QM Alabaster Perfecting Makeup Broad Spectrum SPF 25 OCTINOXATE, TITANIUM DIOXIDE Merle Norman Cosmetics, Inc 551b8c21-3afc-c804-e063-6294a90a5156 2026-06-25 Warnings Exact identifier unii: 15FIX9V2JP Bare Perfecting Makeup Broad Spectrum SPF 25 OCTINOXATE, TITANIUM DIOXIDE Merle Norman Cosmetics, Inc 552f20b2-9a2e-70f3-e063-6394a90a9337 2026-06-25 Warnings Exact identifier unii: 15FIX9V2JP CalaSoothe CALAMINE, MENTHOL, AND ZINC OXIDE Dynarex Corporation 54f12005-acfe-4821-e063-6394a90ac304 2026-06-24 Warnings Exact identifier unii: 1K09F3G675 BROAD SPECTRUM SPF 50 UNIVERSAL TINTED SUNSCREEN TITANIUM DIOXIDE Shantou Woodsleep Biotechnology Co., Ltd. 54fc80b7-8f6c-e2be-e063-6394a90a4b59 2026-06-24 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN A-S Medication Solutions b40f39e4-a37c-4039-ae37-210c1c3c6235 2026-06-23 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM Cerave Developed with Dermatologists Hydrating Sunscreen SPF 30 Body Lightweight, non-greasy feel 3 essential ceramides Mineral Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA Products Inc 54ecaea7-dafe-9694-e063-6394a90ae3b5 2026-06-23 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN TOP CARE (Topco Associates LLC) c62cc12f-5a0e-389a-e053-2995a90a208c 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN TOP CARE (Topco Associates LLC) c6297c23-3b27-c0c6-e053-2995a90a3e76 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN MEIJER DISTRIBUTION INC. a139e495-3dbf-4998-e053-2a95a90ac136 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM pain relief IBUPROFEN Bionpharma Inc. a14ca126-fada-c903-e053-2995a90ae72d 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN HEB ca4be24c-5d92-ddc9-e053-2a95a90aa5a7 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN DOLGENCORP INC 03138a6f-653a-f359-e063-6394a90ac5d6 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN CAPSULE PUBLIX SUPER MARKETS INC 10a6eba7-e400-ce97-e063-6294a90af3bd 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM IBUPROFEN IBUPROFEN DISCOUNT DRUG MART, INC. d07ea9e3-88b0-4aa0-903a-10555dcca37d 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN DISCOUNT DRUG MART, INC. aae40114-343e-12da-e053-2a95a90a9213 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN BJWC 0ca0b6cf-7d1f-4673-b9b9-48f78d80c00a 2026-06-23 Warnings Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.