NDC product
TriDerma Genuine Aloe Burn
NDC 10738-026 · Genuine Virgin Aloe Corporation
Key facts
| Product NDC | 10738-026 |
|---|---|
| Proprietary name | TriDerma Genuine Aloe Burn |
| Nonproprietary name | Aloe Burn Relief |
| Substances | ALLANTOIN |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Genuine Virgin Aloe Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | Jan 1, 2026 |
| 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: