Orajel 4x Medicated Toothache And Gum Cream
NDC Package 10237-888-33
Package Information
Orajel 4x Medicated Toothache And Gum Cream (benzalkonium chloride, benzocaine, menthol, zinc chloride) cream is adults and children 3 years of age and olderapply to affected area up to 4 times daily or as directed by a dentist or doctorchildren between 3 and 12 years of ageshould be supervised in the use of this productchildren under 3 years of agedo not use. This formulation utilizes a cream delivery system. Marketed by Church & Dwight Co., Inc., this product is identified by NDC 10237-888 and is authorized under FDA application M022.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 10237 - Church & Dwight Co., Inc.
- 10237-888 - Orajel 4x Medicated Toothache And Gum Cream
- 10237-888-33 - 1 TUBE in 1 CARTON / 9.4 g in 1 TUBE
- 10237-888 - Orajel 4x Medicated Toothache And Gum Cream
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 10237-888-33 identifies a specific commercial package of 1 tube in 1 carton / 9.4 g in 1 tube of Orajel 4x Medicated Toothache And Gum Cream, a human over the counter drug labeled by Church & Dwight Co., Inc.. This cream is formulated for topical use and contains benzalkonium chloride; benzocaine; menthol, unspecified form; zinc cation as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Church & Dwight Co., Inc. on August 31, 2026. The current certification is valid through December 31, 2027.
How is this Church & Dwight Co., Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10237088833. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.