Home NDC 70518-0761-01 NDC 70518-0761-01 - 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 70518-0761
Requested NDC 70518-0761-01
Package NDCs from labels 70518-0761-0, 70518-0761-1, 70518-0761-2, 70518-0761-3, 70518-0761-4, 70518-0761-5, 70518-0761-6, 70518-0761-7, 70518-0761-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-06-30
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type IBUPROFEN Tablets, USP REMEDYREPACK INC. 2026-06-30 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-0761-0 Ibuprofen 20 in 1 BLISTER PACK TABLET, FILM COATED 20 23 70518-0761-1 Ibuprofen 30 in 1 BLISTER PACK TABLET, FILM COATED 30 23 70518-0761-2 Ibuprofen 28 in 1 BLISTER PACK TABLET, FILM COATED 28 23 70518-0761-3 Ibuprofen 21 in 1 BLISTER PACK TABLET, FILM COATED 21 23 70518-0761-4 Ibuprofen 15 in 1 BLISTER PACK TABLET, FILM COATED 15 23 70518-0761-5 Ibuprofen 10 in 1 BLISTER PACK TABLET, FILM COATED 10 23 70518-0761-6 Ibuprofen 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 23 70518-0761-7 Ibuprofen 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 23
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-0761 IBUPROFEN TABLET, FILM COATED [REMEDYREPACK INC.] 18 Current NDC, Legacy NDC, 8 package rows 20250429_1e6f3ce7-e8a3-40e8-8437-523ef5277b2e.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 155 of 190 · 3,798 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join IBUPROFEN IBUPROFEN TARGET CORPORATION 8e86ae68-7687-79d6-e053-2995a90ac274 2024-01-03 Warnings Exact identifier unii: WK2XYI10QM IBUPROFEN IBUPROFEN TARGET CORPORATION 8e8646fe-fd62-1662-e053-2a95a90a3008 2024-01-03 Warnings Exact identifier unii: WK2XYI10QM IBUPROFEN IBUPROFEN TARGET CORPORATION 8e872c8d-28e2-cd49-e053-2995a90a469f 2024-01-03 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen Mini IBUPROFEN MINI 200 MG TARGET CORPORATION c80426d9-e121-c24d-e053-2a95a90acf2f 2024-01-03 Warnings Exact identifier unii: WK2XYI10QM IBUPROFEN 200 MG IBUPROFEN Basic Drugs, Inc. d3351d44-2078-3adc-e053-2995a90a3c8f 2024-01-03 Warnings Exact identifier unii: WK2XYI10QM Prime Time Daily Protecting Primer SPF 30 SPF 30 PRIME TIME PRIMER Autumn Harp Inc. f2619092-3e7f-5105-e053-2a95a90a3f5a 2024-01-03 Warnings Exact identifier unii: 15FIX9V2JP ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE Amway Corp a1a700b5-d039-4bd2-8420-5c2053095706 2024-01-02 Warnings Exact identifier unii: 15FIX9V2JP Josie Maran Argan Daily Moisturizer SPF47 Protect and Perfect ZINC OXIDE, TITANIUM DIOXIDE Autumn Harp, Inc. cb91c130-45d4-46a0-9628-50e701a6960c 2024-01-02 Boxed warning, Warnings Exact identifier unii: 15FIX9V2JP Discount Drug Mart Eye Drops Multi-Symptom Relief POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE Discount Drug Mart, Inc. 318dc92a-0707-d6a4-e063-6294a90ab78a 2024-01-01 Warnings Exact identifier unii: B697894SGQ Harris Teeter Ultra Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Harris Teeter, LLC. 31ac6883-ffc6-39de-e063-6294a90a52dd 2024-01-01 Warnings Exact identifier unii: B697894SGQ Exchange Select High Performance Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL Army and Air Force Exchange Service 31ac8bd2-c2e9-6f2c-e063-6394a90adc72 2024-01-01 Warnings Exact identifier unii: B697894SGQ CVS Health Fast Acting Lubricant Eye Drops POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL CVS Pharmacy, Inc. 31addfd2-52f2-05b3-e063-6294a90a337f 2024-01-01 Warnings Exact identifier unii: B697894SGQ La Roche Posay New 50 Body and Face SPF 50 Mineral Anthelios Gentle 100 percent mineral UV filters Soft finish with Cell Ox Shield TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA Products Inc c0f7ae46-7161-4d48-9386-007bfafecfd5 2024-01-01 Warnings Exact identifier unii: 15FIX9V2JP La Roche Posay Laboratoire Dermatologique Anthelios HA Mineral Broad Spectrum SPF 30 Daily Moisturizing Sunscreen TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA Products Inc 7bca5947-88a3-4cb3-a6f2-9fa389d344ef 2024-01-01 Warnings Exact identifier unii: 15FIX9V2JP La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Daily Tone Correcting Primer Broad Spectrum SPF 50 Sunscreen TITANIUM DIOXIDE L'Oreal USA Products Inc 89b59bd7-9a91-4b99-84e7-996a8b1d499e 2024-01-01 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen IBUPROFEN Amneal Pharmaceuticals of New York LLC 59f14d2b-f48a-4c25-bea3-3dc9100898b2 2023-12-31 Warnings Exact identifier unii: WK2XYI10QM La Roche Posay Laboratoire Dermatologique Anthelios 50 Tinted Mineral Sunscreen TITANIUM DIOXIDE L'Oreal USA Products Inc 6d3c5fc5-c818-46c4-8db3-cffcdcd56e06 2023-12-31 Warnings Exact identifier unii: 15FIX9V2JP Cerave Developed with Dermatologists Hydrating Sunscreen SPF 50 Face Lightweight, non-greasy feel 3 essential ceramides niacinamide Mineral TITANIUM DIOXIDE AND ZINC OXIDE L'Oreal USA Products Inc bcf5e724-b40a-49dd-8a09-57cefd7f65ad 2023-12-31 Warnings Exact identifier unii: 15FIX9V2JP CeraVe Developed with Dermatologists Sunscreen Broad Spectrum SPF 50 TITANIUM DIOXIDE, ZINC OXIDE L'Oreal USA Products Inc 27d82e37-67ac-4cd3-83c0-fb8388d3a0dd 2023-12-31 Warnings Exact identifier unii: 15FIX9V2JP Ibuprofen Pain Releiver/ Fever Reducer IBUPROFEN Amneal Pharmaceuticals of New York LLC ee241be0-35f8-4789-a71f-98de31d6a590 2023-12-31 Warnings Exact identifier unii: WK2XYI10QM
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.