NDC 82501-1010-00 - 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
- 82501-1010
- Requested NDC
- 82501-1010-00
- Package NDCs from labels
- 82501-1010-0, 82501-1010-00
- Manufacturer
- Gobrands, Inc. (Goodnow)
- Effective date
- 2026-09-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen - Gobrands, Inc. (Goodnow) | Gobrands, Inc. (Goodnow) | 2026-09-01 | 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 | Northwind Health Company, LLC | ab80abe6-f7db-479b-e053-2a95a90a90e3 | 2026-06-12 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| BM BM70 DROPS | ANTIM CURD, FERR MET, PHOSPHORUS, SULPHUR, WIESBADEN, THUJA, VERATRUM ALB | Total Operations Management LLC DBA:Bestmade Natural Products Micro | 54113d1f-e8e7-6b4c-e063-6394a90a0edf | 2026-06-12 | Warnings | 059QF0KO0R |
| BM BM70 DROPS | ANTIM CURD, FERR MET, PHOSPHORUS, SULPHUR, WIESBADEN, THUJA, VERATRUM ALB | BM Private Limited | 53fa21d9-1f80-2e69-e063-6394a90ab9f3 | 2026-06-11 | Warnings | 059QF0KO0R |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | ec6b2df4-2f4f-4601-8b53-0542664e0bd9 | 2026-06-10 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | L.N.K. International, Inc. | 57b39311-bc20-ace6-75a9-a07a9311b373 | 2026-06-09 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Rite Aid Corporation | d9e698f3-c450-4eaa-9cfd-6f48c2656081 | 2026-06-09 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | ARMY AND AIR FORCE EXCHANGE SERVICE | 718a4b73-5f46-4676-afda-f0b4819f5862 | 2026-06-09 | Warnings | WK2XYI10QM |
| XIMONTH Fungi Free Bee Venom Nail Soothing Serum | GLYCERIN | Shantou Ximonth Biotechnology Co., Ltd. | 53bab969-8407-6334-e063-6294a90aa5d1 | 2026-06-08 | Warnings | 059QF0KO0R |
| Ibuprofen | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION, INC. | 68988a5b-7a6a-4ecd-8006-f2610bac2ad7 | 2026-06-08 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | P & L Development, LLC | d0301d0d-fc65-420f-87fd-a08da1584d54 | 2026-06-08 | Warnings | 310964 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Ascend Laboratories, LLC | 9ce036ef-a22d-4fca-9a62-1b10978f7b26 | 2026-06-05 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Aurohealth LLC | 43c94480-78d1-4a23-91d4-1d49fea72cb7 | 2026-06-05 | Warnings | 310964 WK2XYI10QM |
| Ibuprofen Minis | IBUPROFEN | Vivunt Pharma LLC | c46803db-feb7-435c-ac42-cffa99d35f46 | 2026-06-04 | Warnings | 310964 WK2XYI10QM |
| dual action | ACETAMINOPHEN, IBUPROFEN | Publix Super Markets Inc | e185d119-3484-40b1-afb8-6dca49d45e40 | 2026-06-04 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Medline industries, LP | 5d2482b4-cd90-4246-85a9-fd1d35315b6c | 2026-06-04 | Warnings | WK2XYI10QM |
| dual pain reliever | ACETAMINOPHEN, IBUPROFEN | Meijer, Inc. | db1dc4f6-23ec-4a04-baa8-ffa739bce76a | 2026-06-04 | Warnings | WK2XYI10QM |
| DUAL ACTION | ACETAMINOPHEN, IBUPROFEN | Amazon.com Services LLC | 20fe6b3f-e5a6-47d4-a371-9172408fbc46 | 2026-06-04 | Warnings | WK2XYI10QM |
| acetaminophen and ibuprofen | ACETAMINOPHEN, IBUPROFEN | Kroger Company | e6c0cca6-812e-4bea-86b0-e15b10f3f0d4 | 2026-06-04 | Warnings | WK2XYI10QM |
| topcare dual action | ACETAMINOPHEN, IBUPROFEN | Topco Associates LLC | dddc04c4-d500-4d42-8406-89f27a9ad651 | 2026-06-04 | Warnings | WK2XYI10QM |
| Basic Care Ibuprofen | IBUPROFEN | Amazon.com Services LLC | 4c1a1543-a2a2-43fb-901c-cf6bcc374a3f | 2026-06-03 | Warnings | 310964 WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.