NDC product
Daytime Nighttime Cold and Flu
NDC 69256-467 · Harris Teeter, LLC
Key facts
| Product NDC | 69256-467 |
|---|---|
| Proprietary name | Daytime Nighttime Cold and Flu |
| Nonproprietary name | Acetaminophen Dextromethorphan HBr Phenylephrine HCI DoxylamineSucinate |
| Dosage form | KIT |
| Labeler | Harris Teeter, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | May 28, 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: