NDC product
Orajel 4X Medicated Toothache and Gum
NDC 10237-887 · Church & Dwight Co., Inc.
Key facts
| Product NDC | 10237-887 |
|---|---|
| Proprietary name | Orajel 4X Medicated Toothache and Gum |
| Nonproprietary name | Benzalkonium chloride, Benzocaine, Menthol, Zinc chloride |
| Substances | BENZOCAINE, MENTHOL, UNSPECIFIED FORM, BENZALKONIUM CHLORIDE, ZINC CHLORIDE |
| Dosage form | GEL |
| Route | TOPICAL |
| Labeler | Church & Dwight Co., Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| Marketing start | Aug 31, 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: