Vicks DayQuil and Vicks NyQuil
- Product NDC
- 84126-361
- 11-digit product format
- 841260361
- Labeler code
- 84126
- Product ID
- 84126-361_5d6c28ea-515e-b26c-e063-6294a90a035c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr
- Dosage form
- KIT
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-18
- 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
- Vicks DayQuil and Vicks NyQuil
- Brand name suffix
- Intense Flu Rapid Release LiquiCaps
- 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 |
|---|---|---|---|---|---|---|---|
| 84126-361-12 | 84126036112 | 1 KIT in 1 PACKAGE (84126-361-12) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2026-05-18 | No | No | Current |
| 84126-361-48 | 84126036148 | 1 KIT in 1 PACKAGE (84126-361-48) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2026-05-18 | No | No | Current |