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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 20078671-536f-4b0b-a079-f90ac186a670 | 2026-07-03 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| ADVIL | IBUPROFEN | Select Consumer Group | 3ca752d8-957c-21b4-e063-6294a90a5285 | 2026-07-03 | Warnings | WK2XYI10QM |
| Advil Liquigel | IBUPROFEN | Select Consumer Group | 3ca6bc9d-090f-e412-e063-6394a90a6876 | 2026-07-03 | Warnings | WK2XYI10QM |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Ibuprofen | IBUPROFEN | Proficient Rx LP | 34a9b94f-93ba-4a7c-92eb-d0b4b530d887 | 2026-07-02 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Dr. Reddy's Laboratories Inc. | 4d830b9b-b396-9581-7572-c7f19ff17597 | 2026-07-01 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | St. Mary's Medical Park Pharmacy | 88dd304f-1c64-08e3-e053-2a95a90a596f | 2026-07-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | Amazon.com Services LLC | faabb11a-6fa0-492d-85cc-74ff8175b0b3 | 2026-07-01 | Warnings | WK2XYI10QM |
| Infants Motrin | IBUPROFEN | Kenvue Brands LLC | c2302bfe-b367-4867-b803-29f066a42dc7 | 2026-06-30 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 1e6f3ce7-e8a3-40e8-8437-523ef5277b2e | 2026-06-30 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | HAWAII REPACK, INC. | 6239818c-747d-4cbb-9b41-27ca8bbce41b | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Sportpharm LLC | cef04ae4-e78a-454d-bb66-84b1d348c106 | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552d9018-cc7d-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | PDC6A3C0OX |
| Ibuprofen mini dye free | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 552d9018-cc7e-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | WK2XYI10QM |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 552e16b9-f46a-7838-e063-6394a90ab8aa | 2026-06-26 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.