NDC product
Cold Flu Severe Day Night
NDC 72036-186 · Harris Teeter
Key facts
| Product NDC | 72036-186 |
|---|---|
| Proprietary name | Cold Flu Severe Day Night |
| Nonproprietary name | Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride |
| Dosage form | KIT |
| Labeler | Harris Teeter |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Sep 23, 2019 |
| Listing certified through | Dec 31, 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 · Source date: