NDC product
Quality Choice Natural White
NDC 63868-172 · CHAIN DRUG MARKETING ASSOCIATION INC
Key facts
| Product NDC | 63868-172 |
|---|---|
| Proprietary name | Quality Choice |
| Nonproprietary name | Fluoride |
| Substances | SODIUM FLUORIDE, POTASSIUM NITRATE |
| Dosage form | PASTE, DENTIFRICE |
| Route | DENTAL |
| Labeler | CHAIN DRUG MARKETING ASSOCIATION INC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Marketing start | Jan 20, 2011 |
| 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: