Blistex Odor Eaters Medicated Foot
NDC Package 10157-3101-1

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Blistex Odor Eaters Medicated Foot is adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: consult a physician.Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Marketed by Blistex Inc., this product is identified by NDC 10157-3101 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
10157-3101-1
Package Description
142 g in 1 BOTTLE
Product Code
10157-3101
11-Digit Billing Format
10157310101
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Blistex Odor Eaters Medicated Foot
Dosage Form
-
Usage Information
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: consult a physician.Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. For best results apply to affected areas up to 3 or 4 times daily. Sprinkle inside shoes and/or socks for maximum freshness.

Regulatory & Marketing

Labeler Name
Blistex Inc.
FDA Application #
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
02-01-2015
Listing Expiration
12-31-2019
Exclude Flag
I
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 10157-3101-1 identifies a specific commercial package of 142 g in 1 bottle of Blistex Odor Eaters Medicated Foot, labeled by Blistex Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Blistex Inc. on February 01, 2015. The current certification is valid through December 31, 2019.

How is this Blistex Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10157310101. 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)
10157-3101-1
11-Digit CMS (5-4-2)
10157-3101-01

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