NDC product
SPF 50 Daily UV Defense Broad Spectrum Sunscreen
NDC 70484-008 · Vi Medical Products, INC
Key facts
| Product NDC | 70484-008 |
|---|---|
| Proprietary name | SPF 50 Daily UV Defense Broad Spectrum Sunscreen |
| Nonproprietary name | Octinoxate, Zinc Oxide |
| Substances | ZINC OXIDE, OCTINOXATE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Vi Medical Products, INC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Feb 6, 2025 |
| 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: