Meijer Medicated Foot Powder
NDC Package 79481-0043-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Meijer Medicated Foot Powder (menthol) powders is directions ■ Adults and children 2 years of age and over: apply freely up to 3 or 4 times daily ■ Children under 2 years: consult a physician ■ For best results, dry skin thoroughly before use. This formulation utilizes a powder delivery system. Marketed by Meijer Distribution, this product is identified by NDC 79481-0043 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
79481-0043-1
Package Description
283 g in 1 BOTTLE
Product Code
79481-0043
11-Digit Billing Format
79481004301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Meijer Medicated Foot Powder
Non-Proprietary Name
Menthol
Substance Name
Menthol
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
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
Usage Information
Directions ■ Adults and children 2 years of age and over: apply freely up to 3 or 4 times daily ■ Children under 2 years: consult a physician ■ For best results, dry skin thoroughly before use.

Regulatory & Marketing

Labeler Name
Meijer Distribution
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 79481-0043-1 identifies a specific commercial package of 283 g in 1 bottle of Meijer Medicated Foot Powder, a human over the counter drug labeled by Meijer Distribution. This powder is formulated for topical use and contains menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Meijer Distribution on July 01, 2024. The current certification is valid through December 31, 2026.

How is this Meijer Distribution product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481004301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
79481-0043-1
11-Digit CMS (5-4-2)
79481-0043-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.