Daytime Nighttime
- Product NDC
- 11673-474
- 11-digit product format
- 116730474
- Labeler code
- 11673
- Product ID
- 11673-474_537d5541-0fce-6470-e063-6294a90a79e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen Dextromethorphan HBr, Acetaminophen Dextromethorphan HBr Triprolidine HCl
- Dosage form
- KIT
- Labeler
- TARGET CORPORATION
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-01
- 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
- Daytime Nighttime
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4779288a-9850-8490-e063-6394a90abe51 | Available on FDA.report |
DailyMed Product Concepts#
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 |
|---|---|---|---|---|---|---|---|
| 11673-474-64 | 11673047464 | 4 BLISTER PACK in 1 CARTON (11673-474-64) / 1 KIT in 1 BLISTER PACK * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 2026-06-01 | No | No | Current |