DAY TIME NITE TIME INTENSE FLU
- Product NDC
- 79481-4700
- 11-digit product format
- 794814700
- Labeler code
- 79481
- Product ID
- 79481-4700_c261a96e-f3ff-40c6-8aed-87050816c6a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
- Dosage form
- KIT
- Labeler
- Meijer, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-07-01
- 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
- DAY TIME NITE TIME INTENSE FLU
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 6372cbdd-a3a3-499d-91ce-53bcdb83e739 | 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 |
|---|---|---|---|---|---|---|---|
| 79481-4700-2 | 79481470002 | 1 KIT in 1 CARTON (79481-4700-2) * 355 mL in 1 BOTTLE (79481-0110-0) * 355 mL in 1 BOTTLE (79481-0203-0) | 1 kit | 2026-07-01 | No | No | Current |