Home NDC 70000-0175-01 NDC 70000-0175-01 - Leader 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 70000-0175
Requested NDC 70000-0175-01
Package NDCs from labels 70000-0175-1, 70000-0175-2, 70000-0175-3, 70000-0175-5, 70000-0175-4, 70000-0175-7, 70000-0175-6, 70000-0175-8, 70000-0175-9, 70000-0175-01
Manufacturer Cardinal Health 110, LLC. dba Leader
Effective date 2026-02-25
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0175-1 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-1 Leader Ibuprofen 24 in 1 BOTTLE TABLET, FILM COATED 24 14 70000-0175-2 Leader Ibuprofen 50 in 1 BOTTLE TABLET, FILM COATED 50 14 70000-0175-2 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-3 Leader Ibuprofen 100 in 1 BOTTLE TABLET, FILM COATED 100 14 70000-0175-3 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-4 Leader Ibuprofen 250 in 1 BOTTLE TABLET, FILM COATED 250 14 70000-0175-4 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-5 Leader Ibuprofen 500 in 1 BOTTLE TABLET, FILM COATED 500 14 70000-0175-6 Leader Ibuprofen 2 in 1 POUCH TABLET, FILM COATED 2 14 70000-0175-7 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-7 Leader Ibuprofen 120 in 1 BOTTLE TABLET, FILM COATED 120 14 70000-0175-8 Leader Ibuprofen 200 in 1 BOTTLE TABLET, FILM COATED 200 14 70000-0175-8 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14 70000-0175-9 Leader Ibuprofen 250 in 1 BOTTLE TABLET, FILM COATED 250 14 70000-0175-9 Leader Ibuprofen 1 in 1 CARTON TABLET, FILM COATED 1 14
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0175 LEADER IBUPROFEN (IBUPROFEN) TABLET, FILM COATED [CARDINAL HEALTH 110, LLC. DBA LEADER] 12 Current NDC, Legacy NDC, 16 package rows 20240131_d673266c-3d2b-479f-9b53-cdd1b8651393.zip
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 16 of 193 · 3,844 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineral Mattescreen SPF 40 - Untinted TITANIUM DIOXIDE, ZINC OXIDE Supergoop, LLC 08671d39-3be2-d666-e063-6294a90a6207 2026-06-04 Warnings Exact identifier unii: 15FIX9V2JP Mineral Mattescreen SPF 40 - Golden Hour TITANIUM DIOXIDE, ZINC OXIDE Supergoop, LLC c2398820-f003-707f-e053-2a95a90a6929 2026-06-04 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN Medline industries, LP 5d2482b4-cd90-4246-85a9-fd1d35315b6c 2026-06-04 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Epionce Daily Shield Tinted SPF 50 TITANIUM DIOXIDE, ZINC OXIDE Episciences, Inc. 3d1e2921-cba9-4446-e054-00144ff8d46c 2026-06-04 Warnings Exact identifier unii: 15FIX9V2JP dual pain reliever ACETAMINOPHEN, IBUPROFEN Meijer, Inc. db1dc4f6-23ec-4a04-baa8-ffa739bce76a 2026-06-04 Warnings Exact identifier unii: WK2XYI10QM DUAL ACTION ACETAMINOPHEN, IBUPROFEN Amazon.com Services LLC 20fe6b3f-e5a6-47d4-a371-9172408fbc46 2026-06-04 Warnings Exact identifier unii: WK2XYI10QM acetaminophen and ibuprofen ACETAMINOPHEN, IBUPROFEN Kroger Company e6c0cca6-812e-4bea-86b0-e15b10f3f0d4 2026-06-04 Warnings Exact identifier unii: WK2XYI10QM topcare dual action ACETAMINOPHEN, IBUPROFEN Topco Associates LLC dddc04c4-d500-4d42-8406-89f27a9ad651 2026-06-04 Warnings Exact identifier unii: WK2XYI10QM ANESSA PERFECT UV SUNSCREEN SKINCARE MILK GB ZINC OXIDE OCTOCRYLENE ETHYLHEXYL SALICYLATE HOMOSALATE TITANIUM DIOXIDE HONGKONG JIAHE INTERNATIONAL HOLDING LIMITED 5354af18-50c4-5fba-e063-6394a90ace39 2026-06-03 Warnings Exact identifier unii: 15FIX9V2JP BM Silicea Icing Sugar SILICEA ICING SUGAR Total Operations Management LLC DBA:Bestmade Natural Products Micro 535ba100-627f-36b4-e063-6394a90a3373 2026-06-03 Warnings Exact identifier unii: ETJ7Z6XBU4 Rohto Digi-Eye HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE The Mentholatum Company 5d6f37b9-b568-4cb6-92de-eb40779f3f8c 2026-06-03 Warnings Exact identifier unii: 3NXW29V3WO Basic Care Ibuprofen IBUPROFEN Amazon.com Services LLC 4c1a1543-a2a2-43fb-901c-cf6bcc374a3f 2026-06-03 Warnings Exact identifier unii: WK2XYI10QM ATOMY BB SUNSCREEN TITANIUM DIOXIDE, ZINC OXIDE ATOMY CO., LTD. b0cd27ee-4917-4800-bcdf-c6e14b28c1d1 2026-06-02 Warnings Exact identifier unii: 15FIX9V2JP Atomy Sunscreen White Broad Spectrum SPF 50 PLUS HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE ATOMY CO., LTD. ad0b9091-a990-45bf-93f4-d886be1bbffe 2026-06-02 Warnings Exact identifier unii: 15FIX9V2JP Atomy Sunscreen Beige Broad Spectrum SPF 50 PLUS HOMOSALATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE ATOMY CO., LTD. 994d5680-284e-4faf-a29b-4d28f8d46e8f 2026-06-02 Warnings Exact identifier unii: 15FIX9V2JP Matte Veil Tinted Broad Spectrum Sunscreen SPF 40 ZINC OXIDE, TITANIUM DIOXIDE Private Label Skin Care a8d60212-18a7-42af-8bb3-bfcff7690a49 2026-06-02 Warnings Exact identifier unii: 15FIX9V2JP The Mineral Melt SPF30 ZINC OXIDE, TITANIUM DIOXIDE Dune Suncare Inc. 2114fc3b-c8ce-45d2-8a82-4dc54f0adaf3 2026-06-02 Warnings Exact identifier unii: 15FIX9V2JP LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS UV AIR MINERAL SERUM SUNSCREEN BROAD SPECTRUM SPF 50 TITANIUM DIOXIDE AND ZINC OXIDE LOreal USA Products Inc a1acb789-5bf4-4447-b3c5-4a7d4d3013a7 2026-06-01 Warnings Exact identifier unii: 15FIX9V2JP BM Tooth Remineralization CALC PHOS, CALC FLUOR, SILICEA BM Private Limited 5331dc40-2ac8-5fce-e063-6394a90a5875 2026-06-01 Warnings Exact identifier unii: ETJ7Z6XBU4 Period Pills by Biikay ACETAMINOPHEN, IBUPROFEN Kai Squared 40d2ae73-82cf-3fa1-e063-6394a90a9ea2 2026-06-01 Warnings Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.