NDC product
Gillette Clinical Strength All Day Fresh
NDC 37000-286 · Procter and Gamble Manufacturing Company
Key facts
| Product NDC | 37000-286 |
|---|---|
| Proprietary name | Gillette Clinical Strength |
| Labeler | Procter and Gamble Manufacturing Company |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part350 |
| Marketing start | Jul 1, 2008 |
| Marketing end | Nov 25, 2016 |
| Listing certified through | Nov 25, 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: