NDC product
MEDISTIK PROFESSIONAL DUAL ACTION
NDC 50231-221 · Natureteq Inc.
Key facts
| Product NDC | 50231-221 |
|---|---|
| Proprietary name | MEDISTIK PROFESSIONAL DUAL ACTION |
| Nonproprietary name | MENTHOL, METHYL SALICYLATE, EUCALUPTUS |
| Substances | MENTHOL, METHYL SALICYLATE, EUCALYPTUS GLOBULUS LEAF |
| Dosage form | STICK |
| Route | TOPICAL |
| Labeler | Natureteq Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Marketing start | Apr 15, 2011 |
| 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: