NDC product
EltaMD UV Daily
NDC 72043-6804 · CP Skin Health Group, Inc
Key facts
| Product NDC | 72043-6804 |
|---|---|
| Proprietary name | EltaMD UV Daily |
| Nonproprietary name | octinoxate, zinc oxide sunscreen |
| Substances | ZINC OXIDE, OCTINOXATE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | CP Skin Health Group, Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| Marketing start | May 31, 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: