NDC product
TerraFreeze Pain Relief
NDC 71805-855 · Beyond Derma, LLC
Key facts
| Product NDC | 71805-855 |
|---|---|
| Proprietary name | TerraFreeze Pain Relief |
| Nonproprietary name | MENTHOL, METHYL SALICYLATE, HISTAMINE DIHYDROCHLORIDE |
| Substances | MENTHOL, METHYL SALICYLATE, HISTAMINE DIHYDROCHLORIDE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Beyond Derma, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M017 |
| Marketing start | Oct 12, 2017 |
| Listing certified through | Dec 31, 2026 |
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: