daytime nighttime severe cold and flu
- Product NDC
- 72288-813
- 11-digit product format
- 722880813
- Labeler code
- 72288
- Product ID
- 72288-813_94ab8588-ce47-4f59-a89c-3e490c809fbc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan HBr, doxylamine succinate, guaifenesin, phenylephrine HCl
- Dosage form
- KIT
- Labeler
- Amazon.com Services LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-13
- 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
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9bb6bbd5-508e-4781-ad1c-69ccf0a5f13e | 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 |
|---|---|---|---|---|---|---|---|
| 72288-813-02 | 72288081302 | 1 KIT in 1 CARTON (72288-813-02) * 355 mL in 1 BOTTLE (72288-259-40) * 355 mL in 1 BOTTLE (72288-557-40) | 1 kit | 2026-08-13 | No | No | Current |