NDC product
Minoxidil Hair Regrowth Kit
NDC 87813-001 · Guangzhou Zeus E-commerce Co., Ltd
Key facts
| Product NDC | 87813-001 |
|---|---|
| Proprietary name | Minoxidil Hair Regrowth Kit |
| Nonproprietary name | Minoxidil |
| Substances | MINOXIDIL |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Guangzhou Zeus E-commerce 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 | Jun 25, 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: