NDC product
Salicylic Acid
NDC 63941-553 · VALU MERCHANDISERS, CO
Key facts
| Product NDC | 63941-553 |
|---|---|
| Proprietary name | Salicylic Acid |
| Nonproprietary name | Wart Remover Gel Tube |
| Substances | SALICYLIC ACID |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | VALU MERCHANDISERS, CO |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M028 |
| Marketing start | Dec 12, 2017 |
| Marketing end | Jan 20, 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