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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | fef89d3f-16e1-4a76-aabd-11d6eca4be86 | 2026-09-01 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Gobrands, Inc. (Goodnow) | 04e1b176-b74a-413e-a8e1-dd3764b9aa8b | 2026-09-01 | Warnings | WK2XYI10QM |
| equaline dual action pain reliever | ACETAMINOPHEN, IBUPROFEN | United Natural Foods, Inc. dba UNFI | ae0dc3f1-ee6f-4347-af5d-70f45dd68bdb | 2026-08-27 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 2572ed69-d5a7-4513-a202-aca3230e7ec5 | 2026-08-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| foster and thrive dual action | ACETAMINOPHEN, IBUPROFEN | Strategic Sourcing Services LLC | f970d423-1d92-40c0-8358-91d1f963505c | 2026-08-26 | Warnings | WK2XYI10QM |
| Pain Reliever | ACETAMINOPHEN, IBUPROFEN | CVS Pharmacy | 9126e680-d5ff-4189-9f9a-d797822ce670 | 2026-08-26 | Warnings | WK2XYI10QM |
| Leader Dual Action Pain Reliever | ACETAMINOPHEN, IBUPROFEN | Cardinal Health 110, LLC. dba Leader | 2bb1f616-48af-4fe1-9aa9-32fcb2dba50c | 2026-08-26 | Warnings | WK2XYI10QM |
| dual pain reliever | ACETAMINOPHEN, IBUPROFEN | Walgreen Company | 5cb3b0b4-5b47-4ed4-a5e3-f14dbbcb46df | 2026-08-26 | Warnings | WK2XYI10QM |
| Infants Ibuprofen | IBUPROFEN | Walgreens | 3bbbe142-a00c-404b-a116-81ad730ea130 | 2026-08-25 | Warnings | WK2XYI10QM |
| Sterile Water | WATER | REMEDYREPACK INC. | 5dd5d148-6e23-41de-bff5-551b2aea9598 | 2026-08-24 | Warnings, Adverse reactions | 059QF0KO0R |
| Ibuprofen | IBUPROFEN | Major Pharmaceuticals | ba86e936-ef72-43e5-aebf-f2c788fe2266 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Rohto Optic Glow | NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff | 2026-08-20 | Warnings | 6DC9Q167V3 |
| Rohto All-In-One | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE, ZINC SULFATE | The Mentholatum Company | 43e690e4-b381-46e3-838c-33aef5bdadde | 2026-08-20 | Warnings | 3NXW29V3WO |
| Rohto Max Strength | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | e4b49550-1ca3-4bd7-854d-409b53fa5e26 | 2026-08-20 | Warnings | 6OZP39ZG8H |
| Combogesic | ACETAMINOPHEN AND IBUPROFEN | Preferred Pharmaceuticals Inc. | f3cee991-19ef-4a1c-bb14-cbc8b6f32776 | 2026-08-20 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Safeway, Inc. | 57f06daf-690d-44a7-95a5-468732949750 | 2026-08-19 | Warnings | WK2XYI10QM |
| ibuprofen | IBUPROFEN | NuCare Pharmaceuticals,Inc. | 59554a62-3a9a-c0f3-e063-6294a90ad3fd | 2026-08-18 | Warnings | WK2XYI10QM |
| Rohto Preservative Free Dry Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | f4b1974c-2412-45f6-b79d-88b8a0bcb608 | 2026-08-18 | Warnings | 6DC9Q167V3 |
| Rohto Dry-Aid | POVIDONE, PROPYLENE GLYCOL | The Mentholatum Company | 8ea5c6c9-48f4-406a-a2cb-9280c546d87d | 2026-08-18 | Warnings | 6DC9Q167V3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.