NDC product
Dr. Jen SuperPaste Nano-Hydroxyapatite
NDC 84181-735 · Dr Jen Natural, LLC
Key facts
| Product NDC | 84181-735 |
|---|---|
| Proprietary name | Dr. Jen SuperPaste Nano-Hydroxyapatite |
| Nonproprietary name | SODIUM FLUORIDE |
| Substances | SODIUM FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | ORAL |
| Labeler | Dr Jen Natural, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M021 |
| Marketing start | Mar 21, 2024 |
| Listing certified through | Dec 31, 2026 |
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: