Anadent Childrens Kanka Gel
NDC Package 27854-178-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Anadent Childrens Kanka Gel (eugenol) gel is • Adults and children 2 to 12 years of age and older: Moisten a cotton pellet with 1 or 2 drops of the product and then apply to the cotton pellet on the applicable tooth. This formulation utilizes a gel delivery system. Marketed by Belmora Llc, this product is identified by NDC 27854-178 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
27854-178-01
Package Description
1 TUBE in 1 CARTON / 7 g in 1 TUBE
Product Code
27854-178
11-Digit Billing Format
27854017801
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Anadent Childrens Kanka Gel
Non-Proprietary Name
Eugenol
Substance Name
Eugenol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Dental - Administration to a tooth or teeth.
Active Ingredient(s)
EUGENOL 12 mg/g
Pharmacologic Class
Usage Information
• Adults and children 2 to 12 years of age and older: Moisten a cotton pellet with 1 or 2 drops of the product and then apply to the cotton pellet on the applicable tooth. Avoid touching tissues other than the tooth cavity. Apply the dose not more than four times daily or as directed by a dentist or physician.• Children 2 to 12 years of age: should be supervised in the use of this product. Children under 2 years of age: use only under the advice of a dentist or physician.

Regulatory & Marketing

Labeler Name
Belmora Llc
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-08-2022
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 27854-178-01 identifies a specific commercial package of 1 tube in 1 carton / 7 g in 1 tube of Anadent Childrens Kanka Gel, a human over the counter drug labeled by Belmora Llc. This gel is formulated for dental use and contains eugenol 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 Belmora Llc on November 08, 2022. The current certification is valid through December 31, 2026.

How is this Belmora Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 27854017801. 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:

10-Digit Format (5-3-2)
27854-178-01
11-Digit CMS (5-4-2)
27854-0178-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.