NDC product
DG Day Time Cold and Flu Formula and Night Time Cold and Flu Formula
NDC 51013-168 · PuraCap Pharmaceutical LLC
Key facts
| Product NDC | 51013-168 |
|---|---|
| Proprietary name | DG Day Time Cold and Flu Formula and Night Time Cold and Flu Formula |
| Nonproprietary name | acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride |
| Dosage form | KIT |
| Labeler | PuraCap Pharmaceutical LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Jun 15, 2016 |
| 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: