NDC Package 10157-2106-2 Kanka Softbrush

Benzocaine And Zinc Chloride Gel Oral - 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:
10157-2106-2
Package Description:
2 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR
Product Code:
Proprietary Name:
Kanka Softbrush
Non-Proprietary Name:
Benzocaine And Zinc Chloride
Substance Name:
Benzocaine; Zinc Chloride
Usage Information:
Adults and children 2 years of age and older: twist base clockwise to dispense. It may take up to 10 full turns to dispense the initial dose, but subsequent uses should require less than 1 turn.to clean brush tip, rinse with cold waterdry affected area and apply medication by gently brushing the affected area.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 use
11-Digit NDC Billing Format:
10157210602
NDC to RxNorm Crosswalk:
  • RxCUI: 1249105 - benzocaine 20 % / zinc chloride 0.1 % Oral Gel
  • RxCUI: 1249105 - benzocaine 0.2 MG/MG / zinc chloride 0.001 MG/MG Oral Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Blistex Inc
    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):
  • Oral - Administration to or by way of the mouth.
  • 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:
    09-25-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    10157-2106-11 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 10157-2106-2?

    The NDC Packaged Code 10157-2106-2 is assigned to a package of 2 applicator in 1 blister pack / 2 g in 1 applicator of Kanka Softbrush, a human over the counter drug labeled by Blistex Inc. The product's dosage form is gel and is administered via oral form.

    Is NDC 10157-2106 included in the NDC Directory?

    Yes, Kanka Softbrush with product code 10157-2106 is active and included in the NDC Directory. The product was first marketed by Blistex Inc on September 25, 2019 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 10157-2106-2?

    The 11-digit format is 10157210602. 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 5-4-1 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
    5-4-110157-2106-25-4-210157-2106-02