NDC product
Cold Sore Fever Blister Treatment
NDC 21130-605 · Safeway, Inc.
Key facts
| Product NDC | 21130-605 |
|---|---|
| Proprietary name | Cold Sore Fever Blister Treatment |
| Nonproprietary name | Docosanol |
| Substances | DOCOSANOL |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Safeway, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA212385 |
| Marketing start | Jul 31, 2024 |
| Marketing end | 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