NDC product
Studio 35 External Analgesic Medicated Body
NDC 0363-0552 · Walgreen Co
Key facts
| Product NDC | 0363-0552 |
|---|---|
| Proprietary name | Studio 35 External Analgesic Medicated Body |
| Nonproprietary name | Menthol and Zinc Oxide |
| Substances | MENTHOL, ZINC OXIDE |
| Dosage form | POWDER |
| Route | TOPICAL |
| Labeler | Walgreen Co |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Application number | part348 |
| Pharmacologic classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE] |
| Marketing start | Feb 7, 2017 |
| 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: