Derma E Eczema Relief Lotion
NDC Package 54108-8712-1

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

Package Information

Derma E Eczema Relief (oatmeal) lotions is apply as needed to entire body, concentrating on areas of dryness. This formulation utilizes a lotion delivery system. Marketed by Derma E, this product is identified by NDC 54108-8712 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
54108-8712-1
Package Description
175 mL in 1 TUBE
Product Code
54108-8712
11-Digit Billing Format
54108871201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Derma E Eczema Relief
Non-Proprietary Name
Oatmeal
Substance Name
Oatmeal
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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)
OATMEAL 10 mg/mL
Pharmacologic Class
Usage Information
Apply as needed to entire body, concentrating on areas of dryness

Regulatory & Marketing

Labeler Name
Derma E
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-14-2022
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 54108-8712-1 identifies a specific commercial package of 175 ml in 1 tube of Derma E Eczema Relief, a human over the counter drug labeled by Derma E. This lotion is formulated for topical use and contains oatmeal 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 Derma E on June 14, 2022. The current certification is valid through December 31, 2026.

How is this Derma E product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54108871201. 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)
54108-8712-1
11-Digit CMS (5-4-2)
54108-8712-01

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