NDC 85237-1955-01 - Tylenol Sinus Severe
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
- 85237-1955
- Requested NDC
- 85237-1955-01
- Package NDCs from labels
- 85237-1955-0, 85237-1955-1, 85237-1955-2, 85237-1955-3, 85237-1955-4, 85237-1955-6, 85237-1955-7, 85237-1955-01
- Manufacturer
- Select Consumer Group LLC | Select Consumer Group
- Effective date
- 2026-05-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tylenol Sinus Severe - Select Consumer Group LLC | Select Consumer Group | Select Consumer Group LLC | Select Consumer Group | 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.