Vicks DayQuil and Vicks NyQuil
- Product NDC
- 37000-415
- 11-digit product format
- 370000415
- Labeler code
- 37000
- Product ID
- 37000-415_9ba4e766-6095-a56f-e053-2995a90aa126
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Doxylamine Succinate and Guaifenesin
- Dosage form
- KIT
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-07-21
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37000-415-24 | 37000041524 | 1 KIT in 1 PACKAGE (37000-415-24) * 8 BLISTER PACK in 1 CARTON > 2 TABLET in 1 BLISTER PACK * 4 BLISTER PACK in 1 CARTON > 2 TABLET, COATED in 1 BLISTER PACK | 1 kit | 2014-07-21 | 0000-00-00 | No | No | Current |