Vicks DayQuil and Vicks NyQuil
- Product NDC
- 37000-413
- 11-digit product format
- 370000413
- Labeler code
- 37000
- Product ID
- 37000-413_cfe7408f-4167-3641-e053-2a95a90aa8eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Acetaminophen, Doxylamine Succinate, and Dextromethorphan Hydrobromide
- Dosage form
- KIT
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-03-21
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-413-48 | 37000041348 | 1 KIT in 1 PACKAGE (37000-413-48) * 16 BLISTER PACK in 1 CARTON > 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON > 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2014-03-21 | 0000-00-00 | No | No | Current |