NDC product
Nasal Dryness Relief Gel
NDC 10738-051 · Genuine Virgin Aloe Corporation
Key facts
| Product NDC | 10738-051 |
|---|---|
| Proprietary name | Nasal Dryness Relief Gel |
| Nonproprietary name | Allantoin |
| Substances | ALLANTOIN |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Genuine Virgin Aloe Corporation |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | May 20, 2022 |
| 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: