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  5. NDC Package Code: 41250-874-21 Meijer Cold Therapy Roll On

NDC Package 41250-874-21 Meijer Cold Therapy Roll On

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:
41250-874-21
Package Description:
74 mL in 1 BOTTLE
Product Code:
41250-874
Proprietary Name:
Meijer Cold Therapy Roll On
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
Adults and Children 2 years of age and older: rub a thin film over affected areas not more than four times daily; massage not necessary. Children under 2 years of age: Consult physician
11-Digit NDC Billing Format:
41250087421
Billing Unit:
C112160
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:
    Meijer 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):
  • 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 40 mg/mL
    • 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:
    10-22-2018
    End Marketing 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 41250-874-21?

    The NDC Packaged Code 41250-874-21 is assigned to a package of 74 ml in 1 bottle of Meijer Cold Therapy Roll On, a human over the counter drug labeled by Meijer Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 41250-874 included in the NDC Directory?

    Yes, Meijer Cold Therapy Roll On with product code 41250-874 is active and included in the NDC Directory. The product was first marketed by Meijer Inc. on October 22, 2018.

    What is the NDC billing unit for package 41250-874-21?

    The contents of this package are billed C112160

    What is the 11-digit format for NDC 41250-874-21?

    The 11-digit format is 41250087421. 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
    5-3-241250-874-215-4-241250-0874-21