NDC product
Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM Cold and Flu plus Congestion
NDC 58933-550 · Procter & Gamble Manufactura S de RL de CV
Key facts
| Product NDC | 58933-550 |
|---|---|
| Proprietary name | Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM |
| Nonproprietary name | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| Substances | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage form | POWDER, FOR SOLUTION |
| Route | ORAL |
| Labeler | Procter & Gamble Manufactura S de RL de CV |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
| Marketing start | Mar 22, 2023 |
| Marketing end | Jun 30, 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