Vicks DayQuil Severe and Vicks NyQuil Severe
- Product NDC
- 37000-516
- 11-digit product format
- 370000516
- Labeler code
- 37000
- Product ID
- 37000-516_d2034352-89b1-6221-e053-2995a90af467
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Guaifenesin and Doxylamine Succinate
- Dosage form
- KIT
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-10
- 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 |
|---|
| 37000-516-48 | 37000051648 | 1 KIT in 1 PACKAGE (37000-516-48) * 2 BLISTER PACK in 1 CARTON > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK | 1 kit | 2018-07-10 | 0000-00-00 | No | No | Current |