NDC product
Hismile
NDC 83013-317 · Hismile Pty Ltd
Key facts
| Product NDC | 83013-317 |
|---|---|
| Proprietary name | Hismile |
| Nonproprietary name | Grape Bubblegum Flavor Sodium Fluoride Anticavity Toothpaste |
| Substances | SODIUM FLUORIDE |
| Dosage form | GEL |
| Route | DENTAL |
| Labeler | Hismile Pty Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M021 |
| Marketing start | Jan 15, 2024 |
| Listing certified through | Dec 31, 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 · Source date: