NDC 70518-1409-01 - 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
- 70518-1409
- Requested NDC
- 70518-1409-01
- Package NDCs from labels
- 70518-1409-0, 70518-1409-1, 70518-1409-2, 70518-1409-3, 70518-1409-4, 70518-1409-5, 70518-1409-6, 70518-1409-8, 70518-1409-7, 70518-1409-9, 70518-1409-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-07-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IBUPROFEN Tablets, USP | REMEDYREPACK INC. | 2026-07-06 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-1409-0 | Ibuprofen | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | 18 | |
| 70518-1409-1 | Ibuprofen | 21 in 1 BLISTER PACK | TABLET, FILM COATED | 21 | 18 | |
| 70518-1409-2 | Ibuprofen | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | 18 | |
| 70518-1409-3 | Ibuprofen | 14 in 1 BLISTER PACK | TABLET, FILM COATED | 14 | 18 | |
| 70518-1409-4 | Ibuprofen | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | 18 | |
| 70518-1409-5 | Ibuprofen | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 18 | |
| 70518-1409-6 | Ibuprofen | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 18 | |
| 70518-1409-7 | Ibuprofen | 100 in 1 BOX | TABLET, FILM COATED | 100 | 18 | |
| 70518-1409-8 | Ibuprofen | 1 in 1 POUCH | TABLET, FILM COATED | 1 | 18 | |
| 70518-1409-9 | Ibuprofen | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | 18 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-1409 | IBUPROFEN TABLET, FILM COATED [REMEDYREPACK INC.] | 15 | Current NDC, Legacy NDC, 10 package rows | 20250223_421156d2-85dc-4680-b2b4-d15b67539e87.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-1409-0 | EA - Each | 70518-1409 | 4f077557-c8bd-4ff2-b27f-9d6593153c03 | 1 | 2026-01-08 |
| 70518-1409-2 | EA - Each | 70518-1409 | 26e930d5-f673-4bf8-b9a0-3a27ea4b6da4 | 1 | 2026-01-08 |
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 |
|---|---|---|---|---|---|---|
| Pneumo Drops 5018 | PNEUMO DROPS | Professional Complementary Health Formulas | ea6d0286-db1c-48c0-83fd-c18fa8f8629f | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Difficulty Breathing Drops 2171 | DIFFICULTY BREATHING DROPS | Professional Complementary Health Formulas | 30bab475-47dd-4261-b497-1f8edf9dd411 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| RET Spleen/Pancreas 7002 | RET SPLEEN/PANCREAS | Professional Complementary Health Formulas | c6c82d50-0650-4cd9-85b9-c3cd422a35ce | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Vaccinosis Nosode 4004 | VACCINOSIS NOSODE | Professional Complementary Health Formulas | dff675b3-6330-45d0-984c-526a8f44202b | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Sinusitis Drops 2060 | SINUSITIS DROPS | Professional Complementary Health Formulas | 00469764-e0ab-45cf-8e61-6bdc67d31e54 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Large Ring Combination 9302 | LARGE RING COMBINATION | Professional Complementary Health Formulas | cced8a69-7bc0-42ad-b80a-58fc603bf765 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Domestic Animals Nosode Combination 9407 | DOMESTIC ANIMALS NOSODE COMBINATION | Professional Complementary Health Formulas | 222c28aa-e07b-4706-9fb5-585b190f1c5b | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| BADABOOM SUNSCREEN | SUNSCREEN | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47dbf363-2892-4530-e063-6294a90abe1f | 2026-01-08 | Warnings | 15FIX9V2JP |
| ROE WELLNESS SPF 50 MINERAL | SPF 50 MINERAL POWDER | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47dc8155-4abb-4bb7-e063-6294a90af1ad | 2026-01-08 | Warnings | 15FIX9V2JP |
| ALOHA MINERAL BLOCK-BRUSH ON MINERAL | SUNSCREEN SPF50 | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47dd07aa-71b4-5d54-e063-6394a90a4127 | 2026-01-08 | Warnings | 15FIX9V2JP |
| Lubricant Eye Drops Solution | POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL | AvPAK | f5743b38-e3d2-a065-e053-2995a90a4b9a | 2026-01-08 | Warnings | B697894SGQ |
| Anhydrous SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Owen Biosciences, Inc. | 0cc8221d-5ec5-4abf-a4f5-ab06e8dcea68 | 2026-01-08 | Warnings | 15FIX9V2JP |
| HM-B (EDIBLE VINEGAR) | TITANIUM OXIDE | DEMAND SERVICE, CO., LTD. | 9a7b1e74-b8af-449c-e053-2995a90a349e | 2026-01-08 | Warnings | 15FIX9V2JP |
| Cataract Drops 2085 | CATARACT DROPS | Professional Complementary Health Formulas | 6040a096-ccdb-4e1e-a242-be29c3127f27 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| RET Thyroid/Adrenal 7011 | RET THYROID/ADRENAL | Professional Complementary Health Formulas | eb313eb9-4dfc-402e-92b3-14f09f4ba869 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Lymph Stim Liquescence 3016 | LYMPH STIM LIQUESCENCE | Professional Complementary Health Formulas | d91939ea-e3dc-49b1-949a-6618a4c4ae0d | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Nitrogen Combination 9310 | NITROGEN COMBINATION | Professional Complementary Health Formulas | 72a7c0f3-0a57-4aa8-8fe8-a3267b9acd53 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Psorinum Miasm Drops 2054 | PSORINUM MIASM DROPS | Professional Complementary Health Formulas | a34aadab-b634-461f-a0ff-58f42f6e0833 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Xpect Ibuprofen | IBUPROFEN | Cintas Corporation | 976ba88a-6428-40d1-a2fd-eac64963ba1d | 2026-01-08 | Warnings | WK2XYI10QM |
| Pneumonia/Meningitis Nosode Combination 9414 | PNEUMONIA/MENINGITIS NOSODE COMBINATION | Professional Complementary Health Formulas | 823de3e3-4d20-446c-988d-d7a70a747f9a | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.