NDC 70518-0761-01 - 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
- 70518-0761
- Requested NDC
- 70518-0761-01
- 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, 70518-0761-01
- 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 |
|---|---|---|---|---|---|---|
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.