Daytime Nighttime Cold and Flu
- Product NDC
- 72288-744
- 11-digit product format
- 722880744
- Labeler code
- 72288
- Product ID
- 72288-744_5b88e8cd-2fcd-4c22-a4a8-6bb7c401f9fe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
- Dosage form
- KIT
- Labeler
- Amazon.com Services LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-09
- 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 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 |
|---|---|---|---|---|---|---|---|
| 72288-744-72 | 72288074472 | 1 KIT in 1 CARTON (72288-744-72) * 16 BLISTER PACK in 1 KIT (72288-710-32) / 2 TABLET, FILM COATED in 1 BLISTER PACK * 8 BLISTER PACK in 1 KIT (72288-117-16) / 2 TABLET, FILM COATED in 1 BLISTER PACK | 1 kit | 2026-09-09 | No | No | Current |