NDC product
FluoriMax 5000 Sensitive
NDC 57511-0503 · Elevate Oral Care
Key facts
| Product NDC | 57511-0503 |
|---|---|
| Proprietary name | FluoriMax 5000 Sensitive |
| Nonproprietary name | 1.1% Sodium Fluoride with 5% Potassium Nitrate Toothpaste |
| Substances | POTASSIUM NITRATE, SODIUM FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | TOPICAL |
| Labeler | Elevate Oral Care |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Aug 31, 2020 |
| 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: