NDC Package 22431-022-01 Arctic Ice

Menthol 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:
22431-022-01
Package Description:
198 g in 1 BOTTLE
Product Code:
Proprietary Name:
Arctic Ice
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
For the temporary relief of minor muscle aches and pains.See important warnings under "When using this product"not for use on children under 2 years of ageadults & children 2 years & older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.
11-Digit NDC Billing Format:
22431002201
NDC to RxNorm Crosswalk:
  • RxCUI: 311502 - menthol 2 % Topical Gel
  • RxCUI: 311502 - menthol 0.02 MG/MG Topical Gel
  • RxCUI: 311502 - menthol 2 % topical stick
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Blue Cross Laboratories, 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):
    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:
    10-01-2020
    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
    22431-022-02170 g in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 22431-022-01?

    The NDC Packaged Code 22431-022-01 is assigned to a package of 198 g in 1 bottle of Arctic Ice, a human over the counter drug labeled by Blue Cross Laboratories, Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 22431-022 included in the NDC Directory?

    Yes, Arctic Ice with product code 22431-022 is active and included in the NDC Directory. The product was first marketed by Blue Cross Laboratories, Inc. on October 01, 2020 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 22431-022-01?

    The 11-digit format is 22431002201. 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
    5-3-222431-022-015-4-222431-0022-01