NDC product
SPF Lip
NDC 85334-212 · Brent Loftis, D.O., Inc., A California Medical Corporation
Key facts
| Product NDC | 85334-212 |
|---|---|
| Proprietary name | SPF Lip |
| Nonproprietary name | Titanium Dioxide, Zinc Oxide |
| Substances | TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage form | STICK |
| Route | TOPICAL |
| Labeler | Brent Loftis, D.O., Inc., A California Medical Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Marketing start | Apr 19, 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: