Sudafed Sinus Congestion plus Cold Severe Day and Night
- Product NDC
- 50580-660
- 11-digit product format
- 505800660
- Labeler code
- 50580
- Product ID
- 50580-660_5382e4cc-3fc5-359e-e063-6394a90a169b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Diphenhydramine, Pseudoephedrine
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Kenvue Brands LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-10
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sudafed Sinus Congestion plus Cold Severe Day and Night
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5382dcad-0337-4440-e063-6394a90a706e | Available on FDA.report |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 50580-660-16 | 50580066016 | 1 KIT in 1 PACKAGE (50580-660-16) * 2 BLISTER PACK in 1 KIT / 2 TABLET, FILM COATED in 1 BLISTER PACK * 2 BLISTER PACK in 1 KIT / 6 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2026-06-10 | No | No | Current |