NDC product
Daytime Nighttime Cold Flu Relief
NDC 21130-901 · Safeway, Inc.
Key facts
| Product NDC | 21130-901 |
|---|---|
| Proprietary name | Daytime Nighttime Cold Flu Relief |
| Nonproprietary name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCL |
| Dosage form | KIT |
| Labeler | Safeway, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Dec 27, 2019 |
| Marketing end | Dec 27, 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