Gold Bond Medicated Maximum Strength Foot Powder
NDC Package 84714-0171-2

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

Package Information

Gold Bond Medicated Maximum Strength Foot (menthol) powders is ■ adults and children 2 years and older: apply freely up to 3 or 4 times daily  ■ children under 2 years: ask a doctor■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. This formulation utilizes a powder delivery system. Marketed by Gold Bond Co Llc, this product is identified by NDC 84714-0171 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
84714-0171-2
Package Description
283 g in 1 BOTTLE
Product Code
84714-0171
11-Digit Billing Format
84714017102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Gold Bond Medicated Maximum Strength Foot
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
■ adults and children 2 years and older: apply freely up to 3 or 4 times daily  ■ children under 2 years: ask a doctor■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Sprinkle inside shoes for maximum freshness.

Regulatory & Marketing

Labeler Name
Gold Bond Co Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2021
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (84714-0171). Click a package code to view its specific billing and regulatory data.

84714-0171-6
113 g in 1 BOTTLE

* 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 84714-0171-2 identifies a specific commercial package of 283 g in 1 bottle of Gold Bond Medicated Maximum Strength Foot, a human over the counter drug labeled by Gold Bond Co Llc. 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 Gold Bond Co Llc on March 01, 2021. The current certification is valid through December 31, 2026.

How is this Gold Bond Co Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84714017102. 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)
84714-0171-2
11-Digit CMS (5-4-2)
84714-0171-02

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