NDC product
Arizona Sun SPF 45 Sunscreen
NDC 61973-108 · Arizona Sun Products
Key facts
| Product NDC | 61973-108 |
|---|---|
| Proprietary name | Arizona Sun SPF 45 Sunscreen |
| Nonproprietary name | Sunscreen |
| Substances | OCTOCRYLENE, OXYBENZONE, AVOBENZONE, OCTISALATE, HOMOSALATE, OCTINOXATE |
| Dosage form | SPRAY |
| Route | TOPICAL |
| Labeler | Arizona Sun Products |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Feb 20, 2024 |
| 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: