NDC product
Crest Sensitivity Clinical Sensitivity Relief
NDC 37000-512 · The Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 37000-512 |
|---|---|
| Proprietary name | Crest Sensitivity |
| Labeler | The Procter & Gamble Manufacturing Company |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Application number | part356 |
| Marketing start | Aug 30, 2010 |
| Marketing end | Sep 16, 2015 |
| Listing certified through | Sep 16, 2015 |
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: