1. Home
  2. Labeler Index
  3. The Podiatree Co
  4. 54633-414
  5. NDC Package Code: 54633-414-03 K2 Cold Therapy

NDC Package 54633-414-03 K2 Cold Therapy

Menthol Liquid 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:
54633-414-03
Package Description:
88.72 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
54633-414
Proprietary Name:
K2 Cold Therapy
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
Adults and children 12 years of age and older: Apply a thin layer over the affected area not more than 3 to 4 times daily.Children 12 years of age or younger: Consult a doctor.Close cap tightly after use.
11-Digit NDC Billing Format:
54633041403
NDC to RxNorm Crosswalk:
  • RxCUI: 259249 - menthol 10 % Topical Gel
  • RxCUI: 259249 - menthol 0.1 MG/MG Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    The Podiatree Co
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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 10 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:
    05-06-2014
    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 54633-414-03?

    The NDC Packaged Code 54633-414-03 is assigned to a package of 88.72 ml in 1 bottle, with applicator of K2 Cold Therapy, a human over the counter drug labeled by The Podiatree Co. The product's dosage form is liquid and is administered via topical form.

    Is NDC 54633-414 included in the NDC Directory?

    Yes, K2 Cold Therapy with product code 54633-414 is active and included in the NDC Directory. The product was first marketed by The Podiatree Co on May 06, 2014 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 54633-414-03?

    The 11-digit format is 54633041403. 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
    5-3-254633-414-035-4-254633-0414-03