NDC product
ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen
NDC 50390-108 · Amway Corp
Key facts
| Product NDC | 50390-108 |
|---|---|
| Proprietary name | ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen |
| Nonproprietary name | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
| Substances | OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Amway Corp |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Sep 11, 2013 |
| 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: