NDC product
Gillette ClearShield Cool Wave Clear
NDC 69423-744 · The Procter & Gamble Manufacturing Company
Key facts
| Product NDC | 69423-744 |
|---|---|
| Proprietary name | Gillette ClearShield Cool Wave Clear |
| Nonproprietary name | Aluminum Zirconium Octachlorohydrex Gly |
| Substances | ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | The Procter & Gamble Manufacturing Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M019 |
| Marketing start | May 1, 2023 |
| Marketing end | Feb 1, 2028 |
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