NDC product
Daytime Cold, Nighttime Cold multi-symptom
NDC 41163-529 · United Natural Foods, Inc. dba UNFI
Key facts
| Product NDC | 41163-529 |
|---|---|
| Proprietary name | Daytime Cold, Nighttime Cold |
| Nonproprietary name | Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl |
| Dosage form | KIT |
| Labeler | United Natural Foods, Inc. dba UNFI |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Jul 21, 2005 |
| 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: