NDC product
La Roche Posay Laboratoire Dermatologique Anthelios 50 Mineral Ultra Light Sunscreen
NDC 49967-907 · L'Oreal USA Products Inc
Key facts
| Product NDC | 49967-907 |
|---|---|
| Proprietary name | La Roche Posay Laboratoire Dermatologique |
| Nonproprietary name | Titanium dioxide and Zinc oxide |
| Substances | TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | L'Oreal USA Products Inc |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Jul 1, 2011 |
| 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: