NDC product
Rite Aid Maximum Strength
NDC 11822-0316 · Rite Aid
Key facts
| Product NDC | 11822-0316 |
|---|---|
| Proprietary name | Rite Aid |
| Nonproprietary name | Benzocaine |
| Substances | BENZOCAINE |
| Dosage form | GEL, DENTIFRICE |
| Route | ORAL |
| Labeler | Rite Aid |
| 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 | Jan 20, 2011 |
| Marketing end | Nov 30, 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