NDC product
Silver Nitrate Applicators
NDC 12870-0001 · Arzol Chemical Company
Key facts
| Product NDC | 12870-0001 |
|---|---|
| Proprietary name | Silver Nitrate Applicators |
| Nonproprietary name | Silver Nitrate Applicators |
| Substances | POTASSIUM NITRATE, SILVER NITRATE |
| Dosage form | STICK |
| Route | TOPICAL |
| Labeler | Arzol Chemical Company |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jan 1, 1937 |
| 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: