NDC product
Colgate Total Plaque Pro Release Whitening
NDC 35000-181 · Colgate-Palmolive Company
Key facts
| Product NDC | 35000-181 |
|---|---|
| Proprietary name | Colgate Total Plaque Pro Release Whitening |
| Nonproprietary name | Stannous Fluoride |
| Substances | STANNOUS FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | DENTAL |
| Labeler | Colgate-Palmolive Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M021 |
| Marketing start | Nov 9, 2022 |
| Marketing end | Sep 30, 2027 |
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