NDC product
Gillette Clinical Sport Advanced Training Day
NDC 37000-778 · Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 37000-778 |
|---|---|
| Proprietary name | Gillette Clinical Sport Advanced |
| Labeler | Procter & Gamble Manufacturing Company |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part350 |
| Marketing start | Nov 1, 2013 |
| Marketing end | Nov 10, 2016 |
| Listing certified through | Nov 10, 2016 |
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: