NDC Package 70000-0617-1 Leader Roll-on Cooling Pain Relief Topical Analgesic

Menthol,Unspecified Form Gel Topical - 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:
70000-0617-1
Package Description:
74 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
Proprietary Name:
Leader Roll-on Cooling Pain Relief Topical Analgesic
Non-Proprietary Name:
Menthol, Unspecified Form
Substance Name:
Menthol, Unspecified Form
Usage Information:
⬥Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily⬥Children under 2 years of age: consult a doctor.
11-Digit NDC Billing Format:
70000061701
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
74 ML
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:
    Cardinal Health, 110 Dba Leader
    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.
  • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-03-2022
    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 70000-0617-1?

    The NDC Packaged Code 70000-0617-1 is assigned to a package of 74 ml in 1 bottle, with applicator of Leader Roll-on Cooling Pain Relief Topical Analgesic, a human over the counter drug labeled by Cardinal Health, 110 Dba Leader. The product's dosage form is gel and is administered via topical form.This product is billed per "ML" milliliter and contains an estimated amount of 74 billable units per package.

    Is NDC 70000-0617 included in the NDC Directory?

    Yes, Leader Roll-on Cooling Pain Relief Topical Analgesic with product code 70000-0617 is active and included in the NDC Directory. The product was first marketed by Cardinal Health, 110 Dba Leader on November 03, 2022 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 NDC billing unit for package 70000-0617-1?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 74.

    What is the 11-digit format for NDC 70000-0617-1?

    The 11-digit format is 70000061701. 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
    5-4-170000-0617-15-4-270000-0617-01