NDC product
Lasolex AL
NDC 59088-238 · PureTek Corporation
Key facts
| Product NDC | 59088-238 |
|---|---|
| Proprietary name | Lasolex AL |
| Nonproprietary name | MICONAZOLE NITRATE 2% Antifungal |
| Substances | MICONAZOLE NITRATE |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | PureTek Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M005 |
| Pharmacologic classes | Azole Antifungal [EPC], Azoles [CS] |
| Marketing start | Jun 11, 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: