NDC product
Sunceutical SPF 50 Mineral Body Cream
NDC 70157-368 · Baxter Laboratories Pty. Ltd.
Key facts
| Product NDC | 70157-368 |
|---|---|
| Proprietary name | Sunceutical SPF 50 Mineral Body Cream |
| Nonproprietary name | Zinc Oxide |
| Substances | ZINC OXIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Baxter Laboratories Pty. Ltd. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Jan 20, 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: