NDC Package 27854-177-01 Anadent Kanka Gel

Benzocaine Gel Dental - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
27854-177-01
Package Description:
1 TUBE in 1 CARTON / 7 g in 1 TUBE
Product Code:
Proprietary Name:
Anadent Kanka Gel
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Cut open tip of tube on score markAdults and children 2 years of age and older: apply a small amount of product to the cavity and around the gum surrounding the teeth. Use up to 4 times daily or as directed by a dentist or doctorChildren under 12 years of age should be supervised in the use of this productChildren under 2 years of age: do not useĀ 
11-Digit NDC Billing Format:
27854017701
NDC to RxNorm Crosswalk:
  • RxCUI: 238910 - benzocaine 20 % Oral Gel
  • RxCUI: 238910 - benzocaine 0.2 MG/MG Oral Gel
  • RxCUI: 238910 - benzocaine 20 % (180-220 MG per 1 GM) Oral Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Belmora Llc
    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(s):
  • Dental - Administration to a tooth or teeth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    04-15-2022
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 27854-177-01?

    The NDC Packaged Code 27854-177-01 is assigned to a package of 1 tube in 1 carton / 7 g in 1 tube of Anadent Kanka Gel, a human over the counter drug labeled by Belmora Llc. The product's dosage form is gel and is administered via dental form.

    Is NDC 27854-177 included in the NDC Directory?

    Yes, Anadent Kanka Gel with product code 27854-177 is active and included in the NDC Directory. The product was first marketed by Belmora Llc on April 15, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 27854-177-01?

    The 11-digit format is 27854017701. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-227854-177-015-4-227854-0177-01