Triderma Pressure Sore Relief Liquid
NDC Package 10738-031-88

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

Package Information

Triderma Pressure Sore Relief (triderma pressure sore relief wound cleanser) liquids is prevents skin infection, removes germs. This formulation utilizes a liquid delivery system. Marketed by Genuine Virgin Aloe Corporation, this product is identified by NDC 10738-031 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
10738-031-88
Package Description
243 g in 1 BOTTLE, PUMP
Product Code
10738-031
11-Digit Billing Format
10738003188
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Triderma Pressure Sore Relief
Non-Proprietary Name
Triderma Pressure Sore Relief Wound Cleanser
Substance Name
Benzethonium Chloride
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
BENZETHONIUM CHLORIDE .0012 g/g
Usage Information
Prevents skin infection, removes germs

Regulatory & Marketing

Labeler Name
Genuine Virgin Aloe Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2025
Listing Expiration
12-31-2027
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 10738-031-88 identifies a specific commercial package of 243 g in 1 bottle, pump of Triderma Pressure Sore Relief, a human over the counter drug labeled by Genuine Virgin Aloe Corporation. This liquid is formulated for topical use and contains benzethonium chloride 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 Genuine Virgin Aloe Corporation on January 01, 2025. The current certification is valid through December 31, 2027.

How is this Genuine Virgin Aloe Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10738003188. 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)
10738-031-88
11-Digit CMS (5-4-2)
10738-0031-88

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