Home NDC 66689-009-01 NDC 66689-009-01 - 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 66689-009
Requested NDC 66689-009-01
Package NDCs from labels 66689-009-01, 66689-009-50
Manufacturer VistaPharm, Inc.
Effective date 2019-11-01
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Ibuprofen ACTIVE INGREDIENT WK2XYI10QM IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Ibuprofen ACTIVE MOIETY WK2XYI10QM IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Anhydrous Citric Acid INACTIVE INGREDIENT XF417D3PSL IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 D&C Yellow No. 10 INACTIVE INGREDIENT 35SW5USQ3G IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 FD&C Red No. 40 INACTIVE INGREDIENT WZB9127XOA IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Glycerin INACTIVE INGREDIENT PDC6A3C0OX IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Hypromelloses INACTIVE INGREDIENT 3NXW29V3WO IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Polysorbate 80 INACTIVE INGREDIENT 6OZP39ZG8H IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Sodium Benzoate INACTIVE INGREDIENT OJ245FE5EU IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Sucrose INACTIVE INGREDIENT C151H8M554 IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Water INACTIVE INGREDIENT 059QF0KO0R IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Xanthan Gum INACTIVE INGREDIENT TTV12P4NEE IBUPROFEN SUSPENSION [VISTAPHARM, INC.] 2 Ibuprofen ACTIVE INGREDIENT WK2XYI10QM IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Ibuprofen ACTIVE MOIETY WK2XYI10QM IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Anhydrous Citric Acid INACTIVE INGREDIENT XF417D3PSL IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 D&C Yellow No. 10 INACTIVE INGREDIENT 35SW5USQ3G IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 FD&C Red No. 40 INACTIVE INGREDIENT WZB9127XOA IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Glycerin INACTIVE INGREDIENT PDC6A3C0OX IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Hypromelloses INACTIVE INGREDIENT 3NXW29V3WO IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Polysorbate 80 INACTIVE INGREDIENT 6OZP39ZG8H IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Sodium Benzoate INACTIVE INGREDIENT OJ245FE5EU IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Sucrose INACTIVE INGREDIENT C151H8M554 IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Water INACTIVE INGREDIENT 059QF0KO0R IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1 Xanthan Gum INACTIVE INGREDIENT TTV12P4NEE IBUPROFEN SUSPENSION [CARDINAL HEALTH] 1
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 33 of 88 · 1,751 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ibuprofen 200 mg IBUPROFEN R J General Corporation cd3060a5-3b90-42e4-89cd-3b620859045f 2025-11-17 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen 200 mg IBUPROFEN R J General Corporation 1c7221ae-52d1-4d18-b586-c47ff656150d 2025-11-17 Warnings Exact identifier unii: WK2XYI10QM good sense ibuprofen IBUPROFEN Preferred Pharmaceuticals Inc. c447fc6b-e9ef-447a-9609-5f893e18dfa7 2025-11-17 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Family Dollar Services Inc 89ed9311-2185-4660-b219-9ea67b1a71ec 2025-11-15 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Topco Associates, LLC bcf7d4c1-1f99-48df-8f74-9abeefa8d41d 2025-11-15 Warnings Exact identifier unii: WK2XYI10QM Antifungal cream ANTIFUNGAL CREAM Guangzhou Guoyoumi Biotechnology Co Ltd 43a5b3c8-3b99-b113-e063-6394a90a9aff 2025-11-15 Warnings Exact identifier unii: PDC6A3C0OX Ibuprofen IBUPROFEN L.N.K. International, Inc. d1f20e10-0128-f2e5-1a03-6da5d7288a4e 2025-11-15 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN ARMY AND AIR FORCE EXCHANGE SERVICE bf7d0929-a7d5-4164-9c24-566eddcd6489 2025-11-15 Warnings Exact identifier unii: WK2XYI10QM Eyesaline Eyewash Concentrate PURIFIED WATER Honeywell Safety Products USA, Inc. 3765c251-eb14-d60f-e063-6294a90a6a4d 2025-11-12 Warnings Exact identifier unii: 059QF0KO0R Eyesaline Emergency Eyewash PURIFIED WATER Honeywell Safety Products USA, Inc. 37f244fd-c02f-e66a-e063-6394a90aed81 2025-11-12 Warnings Exact identifier unii: 059QF0KO0R Ibuprofen IBUPROFEN P & L Development, LLC ce215099-91b0-43fd-8ac9-17fe6508842c 2025-11-11 Warnings Exact identifier unii: WK2XYI10QM Ibuprofen IBUPROFEN Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) da9d0301-ec14-40c5-b0b9-17096913a849 2025-11-11 Warnings Exact identifier unii: WK2XYI10QM GOODNOW PAIN RELIEF IBUPROFEN Gobrands, Inc 0759085d-6ac3-446b-ac2c-8dc30e32e1d1 2025-11-08 Warnings Exact identifier unii: WK2XYI10QM STERILE WATER WATER Henry Schein, Inc. f4087143-9868-4308-b96c-43657ee8ec28 2025-11-07 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R Atti amour Rose Anti-Aging Repair Classic Essence NIACINAMIDE, GLYCERIN RIVER SUNZ co.,Ltd 1e874ac0-a993-be9e-e063-6394a90af424 2025-11-06 Warnings Exact identifier unii: PDC6A3C0OX Atti amour Rose Anti-Aging Repair Eye Cream NIACINAMIDE, GLYCERIN RIVER SUNZ co.,Ltd 1eeb9c36-5bd8-ec90-e063-6294a90ae4e1 2025-11-06 Warnings Exact identifier unii: PDC6A3C0OX Atti amour Rose Anti-Aging Repair Serum NIACINAMIDE, GLYCERIN RIVER SUNZ co.,Ltd 1eb08f86-eb2a-7f29-e063-6294a90a0516 2025-11-06 Warnings Exact identifier unii: PDC6A3C0OX Atti amour Rose Anti-Aging Repair Moisturizing Cream NIACINAMIDE, GLYCERIN RIVER SUNZ co.,Ltd 1eec4cfe-d5a3-3570-e063-6294a90ac38b 2025-11-06 Warnings Exact identifier unii: PDC6A3C0OX Pranicura 5 GLYCERIN, KAOLIN, CALAMINE, MENTHOL Pranicura Products LLC af520a58-3f3c-4d28-a41f-3ed8f74da095 2025-11-04 Warnings Exact identifier unii: PDC6A3C0OX Bacteriostatic Water BACTERIOSTATIC WATER ProPharma Distribution 42c6938e-f747-ae13-e063-6294a90a59a3 2025-11-04 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.