Menthol Powder
NDC Package 36800-252-10

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

Package Information

Menthol (maximum strength medicated foot powder talc free) powders is adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times dailychildren under 2 years of age, consult a doctorwash and dry feet thoroughlysprinkle powder liberally on feet, between toes and on bottoms of feet. This formulation utilizes a powder delivery system. Marketed by Topco Associates Llc, this product is identified by NDC 36800-252 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
36800-252-10
Package Description
283 g in 1 BOTTLE, PLASTIC
Product Code
36800-252
11-Digit Billing Format
36800025210
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Menthol
Non-Proprietary Name
Maximum Strength Medicated Foot Powder Talc Free
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 2.8 g/283g
Usage Information
Adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times dailychildren under 2 years of age, consult a doctorwash and dry feet thoroughlysprinkle powder liberally on feet, between toes and on bottoms of feet

Regulatory & Marketing

Labeler Name
Topco Associates Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-10-2019
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 36800-252-10 identifies a specific commercial package of 283 g in 1 bottle, plastic of Menthol, a human over the counter drug labeled by Topco Associates 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 Topco Associates Llc on February 10, 2019. The current certification is valid through December 31, 2026.

How is this Topco Associates Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 36800025210. 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 (5-3-2)
36800-252-10
11-Digit CMS (5-4-2)
36800-0252-10

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