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 17 of 192 · 3,834 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen IBUPROFEN Wal-Mart Stores Inc cb897d65-7e98-4d02-be64-0704416a0f29 2026-05-28 Warnings Exact identifier application number: ANDA075010 rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN Family Dollar (FAMILY WELLNESS) 5beb7c11-4ed4-4cd4-9c30-3b0c4016316f 2026-05-27 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Childrens Ibuprofen IBUPROFEN Rite Aid Corporation 1da544eb-ed4e-4124-bea3-f827f1322270 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Family Dollar (FAMILY WELLNESS) da16b1a9-0db2-4f2f-bc85-05ea5ab26e1c 2026-05-27 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Motrin IB IBUPROFEN Select Consumer Group LLC 52c650cf-3085-7b2c-e063-6394a90a797f 2026-05-27 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM ADVIL PM DIPHENHYDRAMINE CITRATE AND IBUPROFEN Select Consumer Group 52c67ae0-707c-851b-e063-6294a90afda4 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM Childrens Ibuprofen IBUPROFEN NuCare Pharmaceuticals, Inc. 52d3e633-13a2-cdcd-e063-6394a90ac189 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM ibuprofen IBUPROFEN Rite Aid Corporation 69ca781a-202e-4579-91e6-f32a22ccc22c 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM Childrens Ibuprofen IBUPROFEN Rite Aid Corporation 5883ebd4-8cf7-45f1-8c66-e87416835fcc 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM ibuprofen IBUPROFEN Rite Aid Corporation 99a76de3-166a-4902-b400-b262a4fa0ae8 2026-05-27 Warnings Exact identifier unii: WK2XYI10QM Calamine CALAMINE AND ZINC OXIDE Pharma Nobis, LLC fbcfa541-beda-06de-e053-6294a90a9298 2026-05-26 Warnings Exact identifier unii: 1K09F3G675 O HUI DAY SHIELD PERFECT SUN BLACK BROAD SPECTRUM SPF 50 SUNSCREEN OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE LG H&H Co., Ltd. 52ba9423-8b9b-38f7-e063-6394a90a95da 2026-05-26 Warnings Exact identifier unii: 15FIX9V2JP IBUPROFEN IBUPROFEN St. Mary's Medical Park Pharmacy 950c3ca7-4481-976f-e053-2995a90ad51e 2026-05-22 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM CHILDRENS IBUPROFEN IBUPROFEN Aurohealth LLC 7461e50d-bfa1-4627-b691-089636b979d2 2026-05-22 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN CVS Pharmacy 121b13c8-0b1a-4c48-9d57-3b53a9228d34 2026-05-22 Warnings Exact identifier unii: WK2XYI10QM Berkley and Jensen Ibuprofen IBUPROFEN BJWC cda57e42-6106-46ee-82d1-479a692ee5bb 2026-05-21 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Mineral SPF 30 Moisturizer MINERAL SPF 30 MOISTURIZER Dont Run Out Inc (DBA: Public Goods) 52462e7e-0c2c-6b64-e063-6394a90a4230 2026-05-21 Warnings Exact identifier unii: 15FIX9V2JP DRMTLGY Radiance Powder TITANIUM DIOXIDE, ZINC OXIDE DRMTLGY 15bda8d5-8c3c-6ba5-e063-6394a90a82d9 2026-05-21 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN Grocery Outlet, Inc. 441d762d-9022-426a-e063-6294a90a5076 2026-05-21 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM SkinCeuticals Future Mineral UV Defense Invisble Sunscreen Mineral Filters Broad Spectrum SPF 50 TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA Products Inc 0b92a940-0dd4-4266-bd47-88c27def62c0 2026-05-20 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.