NDC product
Drs. pharmacy sunscreen SPF 30
NDC 80489-232 · OL PHARMA TECH LLC. (Drs. Pharmacy)
Key facts
| Product NDC | 80489-232 |
|---|---|
| Proprietary name | Drs. pharmacy sunscreen SPF 30 |
| Nonproprietary name | sunscreen SPF 30 |
| Substances | OCTISALATE, HOMOSALATE, AVOBENZONE, OCTOCRYLENE |
| Dosage form | LOTION |
| Route | TOPICAL |
| Labeler | OL PHARMA TECH LLC. (Drs. Pharmacy) |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Jan 1, 2024 |
| 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: