NDC product
Amerfresh Medicated Body Powder
NDC 87510-001 · ONEST LIMITED
Key facts
| Product NDC | 87510-001 |
|---|---|
| Proprietary name | Amerfresh Medicated Body Powder |
| Nonproprietary name | Menthol and Zinc Oxide |
| Substances | MENTHOL, ZINC OXIDE |
| Dosage form | POWDER |
| Route | TOPICAL |
| Labeler | ONEST LIMITED |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M016 |
| Marketing start | Apr 25, 2026 |
| Marketing end | Oct 1, 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