Salicylic Acid Foot Gel
NDC Package 84025-321-01

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

Package Information

Salicylic Acid Foot Gel gel is for daily foot care. This formulation utilizes a gel delivery system. Marketed by Guangzhou Yanxi Biotechnology Co., Ltd, this product is identified by NDC 84025-321 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
84025-321-01
Package Description
100 mL in 1 BOTTLE
Product Code
84025-321
11-Digit Billing Format
84025032101

Clinical Specifications

Proprietary Name
Salicylic Acid Foot Gel
Non-Proprietary Name
Salicylic Acid Foot Gel
Substance Name
Glycerin; Mineral Oil
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For daily foot care

Regulatory & Marketing

Labeler Name
Guangzhou Yanxi Biotechnology Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-09-2025
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 84025-321-01 identifies a specific commercial package of 100 ml in 1 bottle of Salicylic Acid Foot Gel, a human over the counter drug labeled by Guangzhou Yanxi Biotechnology Co., Ltd. This gel is formulated for cutaneous use and contains glycerin; mineral oil 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 Guangzhou Yanxi Biotechnology Co., Ltd on January 09, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Yanxi Biotechnology Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84025032101. 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)
84025-321-01
11-Digit CMS (5-4-2)
84025-0321-01

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