NDC product
Profoot Pain Relief Patches
NDC 29784-601 · Profoot, Inc.
Key facts
| Product NDC | 29784-601 |
|---|---|
| Proprietary name | Profoot Pain Relief Patches |
| Nonproprietary name | CAMPHOR, MENTHOL, METHYL SALICYLATE |
| Dosage form | KIT |
| Labeler | Profoot, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Marketing start | Oct 12, 2023 |
| Marketing end | May 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