NDC product
DMK Ultrascreen Mineral Sunscreen
NDC 81537-282 · Danne Montague King
Key facts
| Product NDC | 81537-282 |
|---|---|
| Proprietary name | DMK Ultrascreen Mineral Sunscreen |
| Nonproprietary name | Zinc Oxide |
| Substances | ZINC OXIDE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | Danne Montague King |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Apr 24, 2025 |
| Listing certified through | Dec 31, 2027 |
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: