NDC product
Aruba Sun SPF 50 Sunscreen
NDC 72839-083 · Derma Care Research Labs, LLC
Key facts
| Product NDC | 72839-083 |
|---|---|
| Proprietary name | Aruba Sun SPF 50 Sunscreen |
| Nonproprietary name | Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10% |
| Substances | OCTISALATE, AVOBENZONE, OCTOCRYLENE, HOMOSALATE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | Derma Care Research Labs, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Nov 25, 2021 |
| 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: