NDC product
5% MINOXIDIL SERUM
NDC 84558-031 · GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Key facts
| Product NDC | 84558-031 |
|---|---|
| Proprietary name | 5% MINOXIDIL SERUM |
| Nonproprietary name | 5% MINOXIDIL SERUM |
| Substances | MINOXIDIL |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Pharmacologic classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
| Marketing start | Aug 20, 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: