NDC product
FRE PROTECT BODY Ultra-Light Gel Cream SPF 50
NDC 69435-1412 · Peer Pharm Ltd.
Key facts
| Product NDC | 69435-1412 |
|---|---|
| Proprietary name | FRE PROTECT BODY Ultra-Light Gel Cream SPF 50 |
| Nonproprietary name | ZINC OXIDE |
| Substances | ZINC OXIDE |
| Dosage form | JELLY |
| Route | TOPICAL |
| Labeler | Peer Pharm Ltd. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Jan 14, 2025 |
| 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: