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 23 of 190 · 3,781 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen PM IBUPROFEN, DIPHENHYDRAMINE HCL MEIJER DISTRIBUTION INC. bb7701aa-f482-69e7-e053-2995a90a71b8 2026-04-17 Warnings Exact identifier unii: WK2XYI10QM YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-DEEP YOUR NAME MINERAL SHEER TINT PML NYC, LLC 0e246e64-2eab-1219-e063-6294a90a79a8 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-FAIR GLOW YOUR NAME MINERAL SHEER TINT PML NYC, LLC 316cd8a3-3d62-83ac-e063-6394a90a4afa 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- HONEY GLOW YOUR NAME MINERAL SHEER TINT PML NYC, LLC 0e2424f4-0011-42b0-e063-6394a90a780d 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-LIGHT YOUR NAME MINERAL SHEER TINT PML NYC, LLC 316cfaea-b71f-2956-e063-6294a90a4f20 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-MEDIUM YOUR NAME MINERAL SHEER TINT PML NYC, LLC 316d1515-6092-a7d6-e063-6394a90ab8b2 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- MEDIUM DEEP YOUR NAME MINERAL SHEER TINT PML NYC, LLC 0e246e70-6ec3-5711-e063-6394a90a3879 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20 YOUR NAME MINERAL SHEER TINT PML NYC, LLC 0e241343-db63-3f1c-e063-6394a90ab538 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20 YOUR NAME MINERAL SHEER TINT PML NYC, LLC 316df5fe-0574-d59f-e063-6294a90af8b9 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- SUN GLOW YOUR NAME MINERAL SHEER TINT PML NYC, LLC 316c5d69-46f4-7677-e063-6294a90a610f 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP Sei Bella Tinted BB Moisturizing Cream 230 N PML NYC, LLC 316ea01b-4bff-55be-e063-6394a90add94 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP Sei Bella Tinted BB Moisturizing Cream 410 N PML NYC, LLC 316e97bc-4b96-ba6e-e063-6294a90a7648 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP EltaMD UV Restore Tinted TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREEN CP Skin Health Group, Inc. 6a48ad0d-20e4-44b1-90d6-30bfbc68a152 2026-04-17 Warnings Exact identifier unii: 15FIX9V2JP ZO Skin Health Daily Mineral Sunshade Broad-Spectrum Sunscreen SPF 45 (Medium) TITANIUM DIOXIDE, ZINC OXIDE ZO Skin Health Inc. 4f95cd0a-f996-648b-e063-6294a90adc28 2026-04-16 Warnings Exact identifier unii: 15FIX9V2JP ZO Skin Health Daily Mineral Sunshade Broad-Spectrum Sunscreen SPF 45 (Tan) TITANIUM DIOXIDE, ZINC OXIDE ZO Skin Health Inc. 4f968058-e851-86d0-e063-6294a90aa786 2026-04-16 Warnings Exact identifier unii: 15FIX9V2JP care one ibuprofen IBUPROFEN American Sales Company d26d2766-6d4c-462b-ae8b-ef8d87acd633 2026-04-16 Warnings Exact identifier unii: WK2XYI10QM Childrens Ibuprofen IBUPROFEN Cardinal Health 107, LLC 9291857c-30b3-414b-99e1-9c127e72c0d4 2026-04-16 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen childrens IBUPROFEN HyVee Inc 55f8def6-f7de-4b3e-a92a-5cd9e68a46a1 2026-04-15 Warnings Exact identifier unii: WK2XYI10QM MELAO Hydrating Mineral Sunscreen TITANIUM DIOXIDE,ZINC OXIDE Guangdong Aimu Biological Technology Co., Ltd 4f778eb0-55f7-38d0-e063-6394a90a69a0 2026-04-15 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN ST. MARY'S MEDICAL PARK PHARMACY 4e67aef4-c3ac-232a-e063-6394a90a3a85 2026-04-15 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.