NDC product
Benzocaine 20%
NDC 0121-1077 · PAI Holdings, LLC dba PAI Pharma
Key facts
| Product NDC | 0121-1077 |
|---|---|
| Proprietary name | Benzocaine 20% |
| Nonproprietary name | Benzocaine 20% |
| Substances | BENZOCAINE |
| Dosage form | SOLUTION |
| Route | TOPICAL |
| Labeler | PAI Holdings, LLC dba PAI Pharma |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Mar 20, 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: