NDC product
Mentholatum Medicated Lip Balm Original
NDC 10742-8865 · The Mentholatum Company
Key facts
| Product NDC | 10742-8865 |
|---|---|
| Proprietary name | Mentholatum Medicated Lip Balm |
| Nonproprietary name | dimethicone, octinoxate, octisalate |
| Substances | DIMETHICONE, OCTINOXATE, OCTISALATE |
| Dosage form | OINTMENT |
| Route | TOPICAL |
| Labeler | The Mentholatum Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M020 |
| Pharmacologic classes | Skin Barrier Activity [PE] |
| Marketing start | Aug 1, 2016 |
| 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: