NDC 85237-1784-01 - ADVIL PM
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
- 85237-1784
- Requested NDC
- 85237-1784-01
- Package NDCs from labels
- 85237-1784-0, 85237-1784-1, 85237-1784-2, 85237-1784-4, 85237-1784-5, 85237-1784-7, 85237-1784-01
- Manufacturer
- Select Consumer Group | Select Consumer Group LLC
- Effective date
- 2026-05-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ADVIL PM - Select Consumer Group | Select Consumer Group LLC | Select Consumer Group | Select Consumer Group LLC | 2026-05-27 | 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 | Preferred Pharmaceuticals Inc. | 06710aef-2631-4925-8e9e-33bae84b5912 | 2025-09-17 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Bryant Ranch Prepack | 86fc38bc-7f54-4aab-9c4d-d0898a4381f9 | 2025-09-17 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Bryant Ranch Prepack | d50f829d-071f-4299-9b74-0f28caac7118 | 2025-09-17 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| CVS SPF 50 Face Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | CVS | 26a69a47-947a-a478-e063-6394a90aa468 | 2025-09-16 | Warnings | 15FIX9V2JP |
| ibuprofen | IBUPROFEN | Meijer Distribution Inc | e28e64dc-5f4e-4260-953a-3de38a5eaa76 | 2025-09-15 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CVS Pharmacy. Inc. | d4336a7c-fb9f-1fbe-e053-2995a90af365 | 2025-09-13 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CVS Pharmacy.Inc. | cd0c3404-9e9d-bfad-e053-2995a90a8719 | 2025-09-13 | Warnings | WK2XYI10QM |
| Owell Naturals Draw Salve, Arnica, Silicea | ARNICA MONTANA HPUS, SILICEA HPUS | Owell Naturals Brand LLC | 1c9dab31-de1f-911b-e063-6294a90a0391 | 2025-09-12 | Warnings | ETJ7Z6XBU4 |
| Owell Naturals Draw Salve | ARNICA MONTANA HPUS, SILICEA HPUS | Owell Naturals Brand LLC | 1536ff1e-16b8-fbbc-e063-6394a90a628e | 2025-09-12 | Warnings | ETJ7Z6XBU4 |
| ibuprofen | IBUPROFEN | A-S Medication Solutions | 7d4ba8be-df59-4a21-8850-8a59bf72b604 | 2025-09-11 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Bryant Ranch Prepack | 894a5d14-e405-43ac-a5a2-0b4de5b28474 | 2025-09-11 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| sunscreen | TITANIUM DIOXIDE(NANO) | Mingyu (guangdong) Cosmetics Technology Co., Ltd | 3e6fe9f3-486b-bba7-e063-6294a90adf37 | 2025-09-10 | Warnings | 15FIX9V2JP |
| Ibuprofen | IBUPROFEN | HEB | acf86f62-1d55-4281-95b7-8b2b51eb7c89 | 2025-09-10 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | HEB | c04ad0b4-5d8a-4861-9eaa-b2aaa7b19664 | 2025-09-10 | Warnings | WK2XYI10QM |
| Green Guard Ibupro relief | IBUPROFEN | Unifirst First Aid Corporation | 2923c4a3-f994-67a7-e054-00144ff8d46c | 2025-09-09 | Warnings | WK2XYI10QM |
| Medique Iprin | IBUPROFEN | Unifirst First Aid Corporation | 2910b50b-c8de-382b-e054-00144ff88e88 | 2025-09-09 | Warnings | WK2XYI10QM |
| Green Guard Ibuprofen Relief | IBUPROFEN | Unifirst First Aid | 0798e401-8247-2fce-e054-00144ff8d46c | 2025-09-09 | Warnings | WK2XYI10QM |
| Medique at Home Iprin | IBUPROFEN | Unifirst First Aid Corporation | b5547f33-2a81-867d-e053-2995a90aa2d0 | 2025-09-09 | Warnings | WK2XYI10QM |
| Medique Iprin | IBUPROFEN | Unifirst First Aid Corporation | 0607edb0-1b3a-2ccd-e054-00144ff8d46c | 2025-09-09 | Warnings | WK2XYI10QM |
| Direct Safety Ibuprofen | IBUPROFEN | Conney Safety Products, LLC | 28d45743-d298-29db-e054-00144ff8d46c | 2025-09-09 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.