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  5. NDC Package Code: 42669-283-01 Maximum Strength Medicated Foot Powder

NDC Package 42669-283-01 Maximum Strength Medicated Foot Powder

Menthol Powder 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:
42669-283-01
Package Description:
283 g in 1 BOTTLE
Product Code:
42669-283
Proprietary Name:
Maximum Strength Medicated Foot Powder
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
Usage Information:
Remove seal beneath cap before first use. Do not use if seal is brokenadults and children 2 years and older - apply freely upto 3 or 4 times dailychildren under 2 years - ask a doctorFor best results, dry skin throughly before applying
11-Digit NDC Billing Format:
42669028301
NDC to RxNorm Crosswalk:
  • RxCUI: 259579 - menthol 1 % Topical Powder
  • RxCUI: 259579 - menthol 0.01 MG/MG Topical Powder
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Davion, Inc
    Dosage Form:
    Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
    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 1 g/100g
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-30-2018
    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 42669-283-01?

    The NDC Packaged Code 42669-283-01 is assigned to a package of 283 g in 1 bottle of Maximum Strength Medicated Foot Powder, a human over the counter drug labeled by Davion, Inc. The product's dosage form is powder and is administered via topical form.

    Is NDC 42669-283 included in the NDC Directory?

    Yes, Maximum Strength Medicated Foot Powder with product code 42669-283 is active and included in the NDC Directory. The product was first marketed by Davion, Inc on January 30, 2018 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 11-digit format for NDC 42669-283-01?

    The 11-digit format is 42669028301. 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
    5-3-242669-283-015-4-242669-0283-01