NDC product
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH
NDC 73242-1126 · DONG IL PHARMS CO.,LTD
Key facts
| Product NDC | 73242-1126 |
|---|---|
| Proprietary name | DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH |
| Nonproprietary name | Silica, Sodium Fluoride, Tocopheryl Acetate, Tetrasodium Pyrophosphate |
| Substances | .ALPHA.-TOCOPHEROL ACETATE, SODIUM PYROPHOSPHATE, SILICON DIOXIDE, SODIUM FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | ORAL |
| Labeler | DONG IL PHARMS CO.,LTD |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jan 2, 2026 |
| 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: