Daytime Nighttime
- Product NDC
- 11673-591
- 11-digit product format
- 116730591
- Labeler code
- 11673
- Product ID
- 11673-591_537c714e-c7eb-3ae8-e063-6394a90ae08c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Guaifenesin and 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 |
|---|---|
| 47a218a0-6395-36bd-e063-6394a90a265a | 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 |
|---|---|---|---|---|---|---|---|
| 11673-591-02 | 11673059102 | 2 BLISTER PACK in 1 CARTON (11673-591-02) / 1 KIT in 1 BLISTER PACK * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2026-06-01 | No | No | Current |