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  5. NDC Package Code: 70612-020-02 Biocool Roll Type

NDC Package 70612-020-02 Biocool Roll Type

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:
70612-020-02
Package Description:
1 CONTAINER in 1 CARTON / 100 mL in 1 CONTAINER (70612-020-01)
Product Code:
70612-020
Proprietary Name:
Biocool Roll Type
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
This product is used as Purpose: BIOCOOL Sports Gel is specially formulated for the temporary activation from muscle and joint stiffness through cooling and refreshing effect. It is patented for the formulation, which contains Menthol, Camphor, and Glycyrrhiza Glabra Root Extract, Methyl sulfonyl methane. Patient response to ultrasound and sports massage therapy is enhanced when BIOCOOL Sports Gel is used to help prior to the ultrasound and massage treatments.
11-Digit NDC Billing Format:
70612002002
NDC to RxNorm Crosswalk:
  • RxCUI: 415974 - menthol 4 % Topical Gel
  • RxCUI: 415974 - menthol 0.04 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Jjindustry.co.ltd
    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 4 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    part348
    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:
    03-02-2016
    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 70612-020-02?

    The NDC Packaged Code 70612-020-02 is assigned to a package of 1 container in 1 carton / 100 ml in 1 container (70612-020-01) of Biocool Roll Type, a human over the counter drug labeled by Jjindustry.co.ltd. The product's dosage form is gel and is administered via topical form.

    Is NDC 70612-020 included in the NDC Directory?

    Yes, Biocool Roll Type with product code 70612-020 is active and included in the NDC Directory. The product was first marketed by Jjindustry.co.ltd on March 02, 2016 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 70612-020-02?

    The 11-digit format is 70612002002. 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
    5-3-270612-020-025-4-270612-0020-02