NDC product
ANTIFUNGAL NAIL
NDC 87710-004 · Guangzhou Huanmei Cosmetics Co., Ltd.
Key facts
| Product NDC | 87710-004 |
|---|---|
| Proprietary name | ANTIFUNGAL NAIL |
| Nonproprietary name | Undecylenic Acid |
| Substances | UNDECYLENIC ACID, TOLNAFTATE |
| Dosage form | LIQUID |
| Route | CUTANEOUS |
| Labeler | Guangzhou Huanmei Cosmetics Co., Ltd. |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Aug 21, 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: