daytime nighttime severe cold and flu
- Product NDC
- 51316-474
- 11-digit product format
- 513160474
- Labeler code
- 51316
- Product ID
- 51316-474_b186a087-530c-41f5-9c61-d9f60370235e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan HBr, doxylamine succinate, guaifenesin, phenylephrine HCl
- Dosage form
- KIT
- Labeler
- CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-20
- 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
- daytime nighttime severe cold and flu
- Listing expiration
- 2027-12-31
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 |
|---|---|---|---|---|---|---|---|
| 51316-474-02 | 51316047402 | 1 KIT in 1 CARTON (51316-474-02) * 355 mL in 1 BOTTLE (51316-415-40) * 355 mL in 1 BOTTLE (51316-681-40) | 1 kit | 2026-08-20 | No | No | Current |