NDC product
DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength
NDC 0363-0463 · Walgreens
Key facts
| Product NDC | 0363-0463 |
|---|---|
| Proprietary name | DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu |
| Nonproprietary name | Daytime Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, NightTime Acetaminophen, Diphenhydramine HCI |
| Dosage form | KIT |
| Labeler | Walgreens |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Mar 31, 2016 |
| Marketing end | Dec 28, 2026 |
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