NDC 59368-232 - Walgreens Pain Reliever Extra Strength
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
- 59368-232
- Package NDCs from labels
- 59368-232-03, 59368-232-01, 59368-232-02
- Manufacturer
- Sixarp, LLC
- Effective date
- 2025-09-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Walgreens Pain Reliever Extra Strength - Sixarp, LLC | Sixarp, LLC | 2025-09-04 | HUMAN OTC DRUG LABEL |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Childrens Mapap | ACETAMINOPHEN | Bryant Ranch Prepack | 69c90cc8-846a-42cf-933a-108671689e8f | 2026-06-05 | Warnings | 362O9ITL9D |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Bryant Ranch Prepack | e83d90f9-513b-47c2-ae2a-748ce775ef5d | 2026-06-05 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| dual action | ACETAMINOPHEN, IBUPROFEN | Publix Super Markets Inc | e185d119-3484-40b1-afb8-6dca49d45e40 | 2026-06-04 | Warnings | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | ASCLEMED USA INC. | 707a9ea7-8f4e-4274-97bd-b8071a0ee06b | 2026-06-04 | Warnings | 362O9ITL9D |
| Medline | ACETAMINOPHEN | Medline Industries, LP | fc5e6f2a-e813-0666-e053-6394a90a66a7 | 2026-06-04 | Warnings | 362O9ITL9D |
| Medline | ACETAMINOPHEN | Medline Industries, LP | fc5d92c2-4bbe-8ad1-e053-6294a90a65b6 | 2026-06-04 | Warnings | 362O9ITL9D |
| acetaminophen | ACETAMINOPHEN | Unit Dose Solutions, Inc. | 537219ac-552a-a30e-e063-6394a90aa9d1 | 2026-06-04 | Warnings | 362O9ITL9D |
| ACETAMINOPHEN AND CODEINE PHOSPHATE | ACETAMINOPHEN AND CODEINE PHOSPHATE | Unit Dose Solutions, Inc. | 537245e8-5e2a-c3e0-e063-6394a90ac858 | 2026-06-04 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| dual pain reliever | ACETAMINOPHEN, IBUPROFEN | Meijer, Inc. | db1dc4f6-23ec-4a04-baa8-ffa739bce76a | 2026-06-04 | Warnings | 362O9ITL9D |
| DUAL ACTION | ACETAMINOPHEN, IBUPROFEN | Amazon.com Services LLC | 20fe6b3f-e5a6-47d4-a371-9172408fbc46 | 2026-06-04 | Warnings | 362O9ITL9D |
| Pain Relief childrens | ACETAMINOPHEN | CVS PHARMACY | ff878f56-125a-4de7-b063-029f7030733d | 2026-06-04 | Warnings | 362O9ITL9D |
| acetaminophen and ibuprofen | ACETAMINOPHEN, IBUPROFEN | Kroger Company | e6c0cca6-812e-4bea-86b0-e15b10f3f0d4 | 2026-06-04 | Warnings | 362O9ITL9D |
| topcare dual action | ACETAMINOPHEN, IBUPROFEN | Topco Associates LLC | dddc04c4-d500-4d42-8406-89f27a9ad651 | 2026-06-04 | Warnings | 362O9ITL9D |
| Childrens Mapap | ACETAMINOPHEN | Major Pharmaceuticals | efec6af2-8b26-47f6-88c8-b0a6d69a2d7d | 2026-06-03 | Warnings | 362O9ITL9D |
| Acetaminophen PM Extra Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | ae3114c3-8cfe-4b81-8ac7-c281fe68b462 | 2026-06-03 | Warnings | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | COSTCO WHOLESALE CORPORATION | 3745aa18-a711-43ed-9bc4-1f087b3c53c0 | 2026-06-03 | Warnings | 362O9ITL9D |
| TYLENOL Extra Strength | ACETAMINOPHEN | Kenvue Brands LLC | 3f653262-b931-7d42-e063-6394a90adddd | 2026-06-03 | Warnings | 362O9ITL9D |
| Rohto Digi-Eye | HYPROMELLOSE, TETRAHYDROZOLINE HYDROCHLORIDE | The Mentholatum Company | 5d6f37b9-b568-4cb6-92de-eb40779f3f8c | 2026-06-03 | Warnings | 3NXW29V3WO |
| Cold and Flu Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | Walgreen Company | de4e8af4-d3d0-44b3-aea3-79016803ccdc | 2026-06-03 | Warnings | 362O9ITL9D |
| Pain Reliever | ACETAMINOPHEN | Walgreen Company | 0b1bef50-7957-4ea1-9ae3-91f59ea2dbb4 | 2026-06-03 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.