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 64 of 188 · 3,759 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Velvet NT Moisturizing Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE SKIN BOSS L.L.C. 35a8508d-7069-c2d6-e063-6394a90a6219 2025-12-15 Exact identifier unii: 15FIX9V2JP Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596fe93-836b-4f8e-e063-6294a90a674a 2025-12-15 Exact identifier unii: 15FIX9V2JP Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359723bb-6152-9566-e063-6294a90a59e0 2025-12-15 Exact identifier unii: 15FIX9V2JP Proper Protection Plus Primer NT TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 3596cd73-0811-32bc-e063-6394a90ad132 2025-12-15 Exact identifier unii: 15FIX9V2JP Proper Protection Plus Primer Tinted TITANIUM DIOXIDE, ZINC OXIDE Skin & Proper LLC 359782d7-6601-7d96-e063-6394a90af9dc 2025-12-15 Exact identifier unii: 15FIX9V2JP Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 37f1b692-0b80-0536-e063-6294a90ae863 2025-12-15 Exact identifier unii: 15FIX9V2JP Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE ESTHETICS BY RIKI LLC 387d5194-bc12-68c1-e063-6394a90ab152 2025-12-15 Exact identifier unii: 15FIX9V2JP Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387c23c2-a9f0-f484-e063-6394a90a4104 2025-12-15 Exact identifier unii: 15FIX9V2JP Tinted Mineral Sun Protectant TITANIUM DIOXIDE, ZINC OXIDE PANDA PAMPERING LLC 387be96f-8cda-ce02-e063-6394a90abea5 2025-12-15 Exact identifier unii: 15FIX9V2JP REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37ede476-43b6-a7c8-e063-6294a90a3e8f 2025-12-15 Exact identifier unii: 15FIX9V2JP REJUVN8 TITANIUM DIOXIDE, ZINC OXIDE FLEUR DE VIE LLC 37efa5e1-e88e-d251-e063-6394a90a9371 2025-12-15 Exact identifier unii: 15FIX9V2JP Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd330bf-92e4-3664-e063-6294a90a0475 2025-12-15 Warnings Exact identifier unii: 15FIX9V2JP Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd37dd1-fd43-7af4-e063-6394a90ae3a0 2025-12-15 Warnings Exact identifier unii: 15FIX9V2JP Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd3dcab-e9fb-0ef5-e063-6394a90acef1 2025-12-15 Warnings Exact identifier unii: 15FIX9V2JP Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE THE BEAUTY ROOM OC INC 3dd40a6a-d52e-ab87-e063-6294a90a966e 2025-12-15 Warnings Exact identifier unii: 15FIX9V2JP Mattifying Skin Primer TITANIUM DIOXIDE, ZINC OXIDE SKIN MAVEN 37662032-2842-1982-e063-6294a90a49a0 2025-12-15 Exact identifier unii: 15FIX9V2JP Deluxe Lip Protection TITANIUM DIOXIDE, ZINC OXIDE BIOHEALTH PLUS LLC 37657895-5fec-82d0-e063-6294a90acf67 2025-12-15 Exact identifier unii: 15FIX9V2JP Facial Mineral Fusion TITANIUM DIOXIDE, ZINC OXIDE IT INTELLIGENT TREATMENT LLC 35944621-e6fb-cd98-e063-6294a90aa641 2025-12-15 Exact identifier unii: 15FIX9V2JP Mineral Mousse TITANIUM DIOXIDE, ZINC OXIDE CLARITY SKIN CARE STUDIO, INC. 35d00778-3857-ce8f-e063-6394a90ab375 2025-12-15 Exact identifier unii: 15FIX9V2JP Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE R. Sonia Batra, MD, Inc. 35933039-8beb-9f98-e063-6394a90a60bb 2025-12-15 Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.