NDC product
Ultra Zinc Mineral Non Tinted
NDC 85357-205 · Skin Therapy Studio LLC
Key facts
| Product NDC | 85357-205 |
|---|---|
| Proprietary name | Ultra Zinc Mineral Non Tinted |
| Nonproprietary name | Zinc Oxide |
| Substances | ZINC OXIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Skin Therapy Studio LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Mar 13, 2024 |
| 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: