NDC 59368-402 - 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
- 59368-402
- Package NDCs from labels
- 59368-402-01
- Manufacturer
- Praxis, LLC
- Effective date
- 2023-01-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen - Praxis, LLC | Praxis, LLC | 2023-01-01 | HUMAN PRESCRIPTION DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Advil PM | DIPHENHYDRAMINE CITRATE, IBUPROFEN | Navajo Manufacturing Company Inc. | a3c30dd2-75f3-4f8b-88d7-4a63dea5bad7 | 2026-04-08 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Discount Drug Mart | cffad7af-44f5-4e54-9e46-c3c5d4ca182f | 2026-04-08 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Lidl US LLC | b840e98e-be1b-496f-9f0d-3a1a55eb9fe4 | 2026-04-08 | Warnings | WK2XYI10QM |
| good sense childrens ibuprofen | IBUPROFEN | L. Perrigo Company | 19253175-4185-468d-9d3d-9b53be764e18 | 2026-04-07 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | L.N.K. International, Inc. | 0ef4913b-5dc3-45bc-9cef-58601f8d2a79 | 2026-04-07 | Warnings | WK2XYI10QM |
| Thera Plus Hemorrhoidal | GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, WHITE PETROLATUM | Fourstar Group USA, Inc. | 5d63bf97-29d2-4c71-97c3-85f425e86207 | 2026-04-07 | Warnings | PDC6A3C0OX |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | PHOENIX RX LLC | 4ee3e849-2197-8883-e063-6394a90a1748 | 2026-04-07 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| LensMate Preservative-Free Artificial Tears | LUBRICANT EYE DROPS | YD BIO USA, INC. | 4ebacb2b-9b2d-6bc1-e063-6294a90a3426 | 2026-04-05 | Warnings | 3NXW29V3WO |
| Exovisse Preservative-Free Artificial Tears | LUBRICANT EYE GEL DROPS | YD BIO USA, INC. | 4ebc154b-128b-9dde-e063-6294a90ae00e | 2026-04-05 | Warnings | 3NXW29V3WO |
| KIDS TOOTHPASTE, FOR CAVITY PROTECTION | KIDS TOOTHPASTE FOR CAVITY PROTECTION | Shulisa (Foshan) Daily ChemicalIndustry Co., Ltd | 4e8fab9e-f05c-5e2f-e063-6294a90aecf9 | 2026-04-03 | Warnings | 059QF0KO0R |
| Ibuprofen Dye-Free | IBUPROFEN | Wal-Mart Stores Inc | 23cb5001-6aeb-434a-b2e8-aaf8bbab9dc6 | 2026-04-01 | Warnings | WK2XYI10QM |
| Care One Ibuprofen PM | DIPHENHYDRAMINE CITRATE AND IBUPROFEN | American Sales Company | d5bf76d1-6fed-4f6b-8507-3e8973295d67 | 2026-04-01 | Warnings | WK2XYI10QM |
| Redness Relief | GLYCERIN, NAPHAZOLINE HCL | Pharmadel LLC | 4c113bb9-814f-d92d-e063-6294a90a8302 | 2026-03-30 | Warnings | PDC6A3C0OX |
| Moisture Oyster | GLYCERIN | Moisture Oyster Inc | 4e45317a-437f-4d88-e063-6294a90a98d0 | 2026-03-30 | Warnings | PDC6A3C0OX |
| Ibuprofen | IBUPROFEN | Bryant Ranch Prepack | 1ebf94fb-76b6-4c01-be1b-575062827545 | 2026-03-30 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN ORAL | Aurobindo Pharma Limited | 758eeb45-e599-4c1a-969d-8fa33f27bf14 | 2026-03-30 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| ibuprofen pm | DIPHENHYDRAMINE CITRATE, IBUPROFEN | Rite Aid Corporation | d9eefb84-cc2e-4deb-a1c0-a7c21929f5ac | 2026-03-27 | Warnings | WK2XYI10QM |
| Aveeno Skin Relief Healing | GLYCERIN | Kenvue Brands LLC | 345fdde5-700b-7103-e063-6394a90a0e3e | 2026-03-27 | Warnings | PDC6A3C0OX |
| Ibuprofen Oral | IBUPROFEN ORAL | Camber Consumer Care Inc | b2dd4863-613e-4a41-98c1-3191e41b8463 | 2026-03-26 | Warnings | WK2XYI10QM |
| Crocodile Tears Lubricant Eye Drops | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | Crocodile Tears LLC | 4df29336-ea0c-0484-e063-6294a90a685a | 2026-03-26 | Warnings | PDC6A3C0OX 3NXW29V3WO |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.