NDC 70518-0761-04 - 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
- 70518-0761
- Requested NDC
- 70518-0761-04
- Package NDCs from labels
- 70518-0761-0, 70518-0761-1, 70518-0761-2, 70518-0761-3, 70518-0761-4, 70518-0761-5, 70518-0761-6, 70518-0761-7, 70518-0761-04
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-06-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IBUPROFEN Tablets, USP | REMEDYREPACK INC. | 2026-06-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-0761-0 | Ibuprofen | 20 in 1 BLISTER PACK | TABLET, FILM COATED | 20 | 23 | |
| 70518-0761-1 | Ibuprofen | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 23 | |
| 70518-0761-2 | Ibuprofen | 28 in 1 BLISTER PACK | TABLET, FILM COATED | 28 | 23 | |
| 70518-0761-3 | Ibuprofen | 21 in 1 BLISTER PACK | TABLET, FILM COATED | 21 | 23 | |
| 70518-0761-4 | Ibuprofen | 15 in 1 BLISTER PACK | TABLET, FILM COATED | 15 | 23 | |
| 70518-0761-5 | Ibuprofen | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 23 | |
| 70518-0761-6 | Ibuprofen | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 23 | |
| 70518-0761-7 | Ibuprofen | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | 23 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-0761 | IBUPROFEN TABLET, FILM COATED [REMEDYREPACK INC.] | 18 | Current NDC, Legacy NDC, 8 package rows | 20250429_1e6f3ce7-e8a3-40e8-8437-523ef5277b2e.zip |
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 |
|---|---|---|---|---|---|---|
| Meijer Multi-Symptom Relief | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | Meijer, Inc. | e7a5677a-ff33-c039-e053-2a95a90ae6c7 | 2025-12-30 | Warnings | B697894SGQ |
| Avenova Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | NovaBay Pharmaceuticals, Inc. | cd17f037-5aa5-0ef8-e053-2a95a90a39cb | 2025-12-30 | Warnings | B697894SGQ |
| Equate Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Walmart, Inc. | deebaf7f-f20d-4d7f-e053-2a95a90a4b4f | 2025-12-30 | Warnings | B697894SGQ |
| Equate Multi-Symptom Relief Eye Drops | POLYETHYLENE GLYCOL 400,TETRAHYDROZOLINE HCL, ZINC SULFATE | Walmart, Inc. | eb8ed76b-9cd7-3636-e053-2a95a90a9583 | 2025-12-30 | Warnings | B697894SGQ |
| CorneaCare Recover Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | CorneaCare Inc. | 1fd3a5ed-8963-5c8e-e063-6394a90a6527 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Chain Drug Marketing Assoc., Inc. | 0cd1b36a-a07a-a1db-e063-6294a90a5994 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Moisturizing Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Chain Drug Marketing Association, Inc. | 1fb81759-5931-59c8-e063-6294a90a2277 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Lubricant Eye Drops Long Lasting | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Chain Drug Marketing Assoc., Inc. | 0cd91c45-88a2-f88c-e063-6294a90ad127 | 2025-12-30 | Warnings | B697894SGQ |
| Archies Dry Eye Relief | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Archie's Remedies | 07da099b-6b7f-984d-e063-6294a90a12ac | 2025-12-30 | Warnings | B697894SGQ |
| Equaline Multi-Symptom Eye Drops | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | United Natural Foods, Inc. | fe467606-6d66-b695-e053-6294a90aab5d | 2025-12-30 | Warnings | B697894SGQ |
| IBUPROFEN | IBUPROFEN | TIME CAP LABORATORIES, INC | e0a8315a-80a5-4be3-aad1-3d01f00df494 | 2025-12-29 | Warnings | WK2XYI10QM |
| SPF 30 Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE | CLEURE | f5512f34-08ee-b0f6-e053-2a95a90ab5bd | 2025-12-29 | Warnings | 15FIX9V2JP |
| RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 | OCTINOXATE AND TITANIUM DIOXIDE | ESTEE LAUDER INC | 897b8edb-f089-4a49-baca-e05806b0a068 | 2025-12-29 | Warnings | 15FIX9V2JP |
| OI LIN SUNMILK SUNSCREEN SPF 30 | SUNSCREEN, TITANIUM DIOXIDE | Sunrider Manufacturing L.P. | 26b57314-1616-4ca4-b65f-a363c525b432 | 2025-12-29 | Warnings | 15FIX9V2JP |
| Medicated Cornstarch Baby Powder | ACTIVE CORN STARCH | Davion, Inc. | e39032d1-c8cd-4a41-af10-126970b8ad38 | 2025-12-29 | Warnings | O8232NY3SJ |
| 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 | ANDA091625 197806 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | ab074ae8-5696-5327-e053-2a95a90a7ce3 | 2025-12-26 | Boxed warning, Warnings, Adverse reactions | ANDA091625 197805 WK2XYI10QM |
| Childrens Ibuprofen Oral Suspension | IBUPROFEN | AptaPharma Inc. | 40936019-74ab-4b25-a502-7bbc6e12034a | 2025-12-26 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.