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  5. NDC Package Code: 35192-039-02 Kanjo Pain Relief Gel

NDC Package 35192-039-02 Kanjo Pain Relief Gel

Menthol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
35192-039-02
Package Description:
120 g in 1 TUBE
Product Code:
35192-039
Proprietary Name:
Kanjo Pain Relief Gel
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
Apply generous amount of gel directly affected area massage into painful area until thoroughly absorbed into skin
11-Digit NDC Billing Format:
35192003902
NDC to RxNorm Crosswalk:
  • RxCUI: 415975 - menthol 5 % Topical Gel
  • RxCUI: 415975 - menthol 0.05 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ca-botana International
    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):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • MENTHOL 6 g/120g
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-31-2020
    Listing Expiration Date:
    12-31-2025
    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 35192-039-02?

    The NDC Packaged Code 35192-039-02 is assigned to a package of 120 g in 1 tube of Kanjo Pain Relief Gel, a human over the counter drug labeled by Ca-botana International. The product's dosage form is gel and is administered via topical form.

    Is NDC 35192-039 included in the NDC Directory?

    Yes, Kanjo Pain Relief Gel with product code 35192-039 is active and included in the NDC Directory. The product was first marketed by Ca-botana International on August 31, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 35192-039-02?

    The 11-digit format is 35192003902. 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
    5-3-235192-039-025-4-235192-0039-02