NDC product
Multi-Purrose Nail
NDC 87240-364 · Jiangxi Zhongteng Pharmaceutical Co., Ltd
Key facts
| Product NDC | 87240-364 |
|---|---|
| Proprietary name | Multi-Purrose Nail |
| Nonproprietary name | Multi-Purrose Nail |
| Substances | TOLNAFTATE |
| Dosage form | SOLUTION |
| Route | CUTANEOUS |
| Labeler | Jiangxi Zhongteng Pharmaceutical Co., Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Nov 20, 2025 |
| 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: