NDC product
DayQuil VapoCOOL SEVERE COLD and FLU plus CONGESTION
NDC 69423-990 · The Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 69423-990 |
|---|---|
| Proprietary name | DayQuil VapoCOOL SEVERE |
| Nonproprietary name | acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin |
| Substances | PHENYLEPHRINE HYDROCHLORIDE, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | The Procter & Gamble Manufacturing Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA] and 3 more |
| Marketing start | Mar 22, 2021 |
| Listing certified through | Dec 31, 2027 |
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: