NDC product
LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g
NDC 85948-251 · DONGDONGGURIMOO CO.,LTD.
Key facts
| Product NDC | 85948-251 |
|---|---|
| Proprietary name | LEBELAGE UV SUN ULTRA SHIELD SUN SCREENLOTION 50g |
| Nonproprietary name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTOCRYLENE, OCTISALATE |
| Substances | AVOBENZONE, OCTINOXATE, OCTOCRYLENE, HOMOSALATE, OCTISALATE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | DONGDONGGURIMOO CO.,LTD. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Jan 12, 2026 |
| 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: