NDC 70518-4341-01 - 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
- 70518-4341
- Requested NDC
- 70518-4341-01
- Package NDCs from labels
- 70518-4341-0, 70518-4341-1, 70518-4341-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-09-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen Tablets, USP Rx only | REMEDYREPACK INC. | 2026-09-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-4341-0 | Ibuprofen | 30 in 1 BLISTER PACK | TABLET | 30 | 2 | |
| 70518-4341-1 | Ibuprofen | 30 in 1 BLISTER PACK | TABLET | 30 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-4341 | IBUPROFEN TABLET [REMEDYREPACK INC.] | 1 | Current NDC, 2 package rows | 20250523_2144eff0-d7ab-486d-b116-a4ff3ae2afe2.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 |
|---|---|---|---|---|---|---|
| IBUPROFEN | IBUPROFEN | Harris Teeter | 9d5c994a-8363-4ddb-956c-e12b79a32a58 | 2026-07-29 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Harris Teeter | 87ffbf01-54de-45a8-b2a3-367d21927882 | 2026-07-29 | Warnings | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | Harris Teeter | 14515409-736f-4119-b6a0-cb19ee2e948e | 2026-07-29 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Harris Teeter | 1fa28cb4-ae7b-4fa9-ae64-9bd8ccfcc633 | 2026-07-29 | Warnings | WK2XYI10QM |
| ADVIL PM | DIPHENHYDRAMINE HCL, IBUPROFEN | Haleon US Holdings LLC | 405afdb4-c157-1d88-f232-848063ba4714 | 2026-07-29 | Warnings | WK2XYI10QM |
| ADVIL COLD AND SINUS | IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE | Haleon US Holdings LLC | 0da9ed22-bfb4-d61b-110b-0c7760332a98 | 2026-07-29 | Warnings | WK2XYI10QM |
| ADVIL MIGRAINE | IBUPROFEN | Haleon US Holdings LLC | e4a6219d-4ad4-0119-4cf8-7fc39b4b5979 | 2026-07-29 | Warnings | WK2XYI10QM |
| Advil | IBUPROFEN | Haleon US Holdings LLC | 1f01c10a-9434-91a4-2ee4-352315a6b610 | 2026-07-29 | Warnings | WK2XYI10QM |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Ascend Laboratories, LLC | 4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | H E B | 21567c0f-abba-4a40-a0b9-5ce49b3d9648 | 2026-07-28 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | PD-Rx Pharmaceuticals, Inc. | 656658cc-8cf0-42b6-af4f-4e3ab7648625 | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | 197807 WK2XYI10QM |
| Polyethylene Glycol 3350 | INSTALAX POLYETHYLENE GLYCOL 3350 | Sun Pharmaceutical Industries, Inc. | 40bd1be7-de67-8dff-e063-6294a90aca95 | 2026-07-24 | Warnings | G2M7P15E5P |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | a7756b22-73cf-4262-aa8e-0577ddecd03b | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 197805 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | 1ca722bb-940e-4b3e-9561-d87e2feb1ff8 | 2026-07-24 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Shield Pharmaceuticals Corp | fc6c29b4-f1b3-4cfe-8c96-564d083be39c | 2026-07-24 | Warnings | WK2XYI10QM |
| ESIKA COLORFIX POLVOS 32H POLVO COMPACTO FACIAL DE ALTA COBERTURA FPS 15 110-C | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | BEL STAR S.A. | 575fb2c3-e332-8a3b-e063-6394a90a9fd9 | 2026-07-24 | Warnings | 15FIX9V2JP |
| childrens ibuprofen | IBUPROFEN | Rite Aid Corporation | 26bccfc1-bc8d-4241-a078-c760048951c9 | 2026-07-24 | Warnings | WK2XYI10QM |
| PEG 3350 and Electrolytes | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE | A-S Medication Solutions | 19daf830-7270-4661-81b1-ded38f867f28 | 2026-07-24 | Warnings, Adverse reactions | G2M7P15E5P |
| IBUPROFEN | IBUPROFEN | HF Acquisition Co LLC, DBA HealthFirst | 574b6f15-70bc-fca7-e063-6294a90a0455 | 2026-07-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Safeway, Inc. | a530d43d-e9c4-4edb-af66-c92860e46f45 | 2026-07-23 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.