NDC product
Vicks DayQuil Cold and Flu Multi-Symptom Relief
NDC 37000-555 · The Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 37000-555 |
|---|---|
| Proprietary name | Vicks DayQuil |
| Labeler | The Procter & Gamble Manufacturing Company |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Jun 22, 2011 |
| Marketing end | Nov 1, 2023 |
| Listing certified through | Nov 1, 2023 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: