NDC 85237-1832-01 - Aleve Caplets
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
- 85237-1832
- Requested NDC
- 85237-1832-01
- Package NDCs from labels
- 85237-1832-0, 85237-1832-1, 85237-1832-2, 85237-1832-4, 85237-1832-6, 85237-1832-7, 85237-1832-01
- Manufacturer
- Select Consumer Group
- Effective date
- 2026-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aleve Caplets - Select Consumer Group | Select Consumer Group | 2026-07-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85237-1832-1 | AleveCaplets | 1 in 1 BLISTER PACK | TABLET | 1 | 2 | |
| 85237-1832-1 | AleveCaplets | 1 in 1 POUCH | TABLET | 1 | 2 | |
| 85237-1832-2 | AleveCaplets | 2 in 1 BLISTER PACK | TABLET | 2 | 2 | |
| 85237-1832-2 | AleveCaplets | 1 in 1 POUCH | TABLET | 1 | 2 | |
| 85237-1832-4 | AleveCaplets | 1 in 1 POUCH | TABLET | 1 | 2 | |
| 85237-1832-4 | AleveCaplets | 25 in 1 BOX, UNIT-DOSE | TABLET | 25 | 2 | |
| 85237-1832-6 | AleveCaplets | 50 in 1 BOX, UNIT-DOSE | TABLET | 50 | 2 | |
| 85237-1832-6 | AleveCaplets | 1 in 1 POUCH | TABLET | 1 | 2 |
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.
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|---|---|---|---|---|---|---|
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| DOCTRUST ONE S Tooth | SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE | DONG IL PHARMS CO.,LTD | 4476923a-48f1-9f72-e063-6394a90a0708 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 44768dd1-b132-c33b-e063-6294a90accd4 | 2025-11-25 | Warnings | ETJ7Z6XBU4 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.