NDC 59368-003 - up and up dye free infants concentrated 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
- 59368-003
- Package NDCs from labels
- 59368-003-01, 59368-003-02
- Manufacturer
- Sixarp, LLC
- Effective date
- 2024-03-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| up and up dye free infants concentrated ibuprofen - Sixarp, LLC | Sixarp, LLC | 2024-03-15 | HUMAN OTC 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 |
|---|---|---|---|---|---|---|
| Equate Optimal Hydration Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Walmart, Inc. | 151b9723-5d5e-ac2b-e063-6294a90af073 | 2025-12-30 | Warnings | PDC6A3C0OX |
| IBUPROFEN | IBUPROFEN | TIME CAP LABORATORIES, INC | e0a8315a-80a5-4be3-aad1-3d01f00df494 | 2025-12-29 | Warnings | WK2XYI10QM |
| OCUFRESH | WATER | Optics Laboratory Inc. | b8e477a9-66b9-496b-92fb-3d4bbd7b36b5 | 2025-12-29 | Warnings | 059QF0KO0R |
| Kollourion Eyesalve Eyewash | PURIFIED WATER 98.3% | Miracle Eye Pharmaceuticals | b56d2ab9-169b-b490-e053-2a95a90a80b3 | 2025-12-28 | Warnings | 059QF0KO0R |
| Childrens Ibuprofen Oral Suspension Original Berry Flavor | IBUPROFEN | Puro Pharma Inc. | 6b993b25-9c81-4d75-b332-6de3f6c3b4c9 | 2025-12-27 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | a8b46ae5-67bc-494d-850e-b4e4ed5a33b3 | 2025-12-27 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | f2a08223-a73a-5461-e053-2995a90a3bce | 2025-12-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | ab074ae8-5696-5327-e053-2a95a90a7ce3 | 2025-12-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Childrens Ibuprofen Oral Suspension | IBUPROFEN | AptaPharma Inc. | 40936019-74ab-4b25-a502-7bbc6e12034a | 2025-12-26 | Warnings | WK2XYI10QM |
| Childrens Ibuprofen Grape | IBUPROFEN | AptaPharma Inc. | 7caca7e2-6652-45fc-9538-275b43a1594e | 2025-12-26 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd | 46a9424c-fd7d-f88b-e063-6294a90abceb | 2025-12-24 | Warnings | WK2XYI10QM |
| Lil Drug Store Ibuprofen | IBUPROFEN | Lil Drug Store Products, Inc | 29190ebf-bb9c-4406-be7b-4427741aeb74 | 2025-12-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CVS | 10424ad8-74fc-4f5f-e063-6394a90a13bd | 2025-12-23 | Warnings | WK2XYI10QM |
| good sense ibuprofen childrens | IBUPROFEN | Preferred Pharmaceuticals Inc. | 7ac61180-d668-4eec-b04f-d14f7b552a4d | 2025-12-23 | Warnings | WK2XYI10QM |
| Hydrocodone Bitartrate and Ibuprofen | HYDROCODONE BITARTRATE AND IBUPROFEN | Aurolife Pharma, LLC | 470df63a-5c0f-42df-9023-a330a901153e | 2025-12-23 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Motrin IB Migraine | IBUPROFEN | Kenvue Brands LLC | 34818110-5291-4bda-9571-bd77d90bba7c | 2025-12-22 | Warnings | WK2XYI10QM |
| Motrin IB | IBUPROFEN | Kenvue Brands LLC | d9fc716a-fba5-45f8-8024-52325799d1dd | 2025-12-22 | Warnings | WK2XYI10QM |
| Equate Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Hanlim | 46851e7c-8910-6456-e063-6394a90abafb | 2025-12-22 | Warnings | PDC6A3C0OX |
| Ibuprofen | IBUPROFEN | Granules USA, Inc. | 8cb595d2-b7c2-687d-e053-2a95a90a5720 | 2025-12-22 | Warnings | WK2XYI10QM |
| Redness and Dry Eye Relief | GLYCERIN, NAPHAZOLINE HYDROCHLORIDE | KC Pharmaceuticals, Inc | 4682f68d-6bdd-d860-e063-6394a90a2b52 | 2025-12-21 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.