North Woods Derma Foam E-2 Soap
NDC Package 53125-817-29

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

Package Information

North Woods Derma Foam E-2 (benzalkonium chloride) soaps is usesFor handwashing to decrease the bacteria on the skin.Recommended for repeated use. This formulation utilizes a soap delivery system. Marketed by Superior Chemical Corporation, this product is identified by NDC 53125-817 and is authorized under FDA application 505G(a)(3).

Identification & Billing

NDC Package Code
53125-817-29
Package Description
1000 mL in 1 BAG
Product Code
53125-817
11-Digit Billing Format
53125081729
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
North Woods Derma Foam E-2
Non-Proprietary Name
Benzalkonium Chloride
Substance Name
Benzalkonium Chloride
Dosage Form
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
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)
BENZALKONIUM CHLORIDE 1.3 mg/mL
Usage Information
UsesFor handwashing to decrease the bacteria on the skin.Recommended for repeated use.

Regulatory & Marketing

Labeler Name
Superior Chemical Corporation
Product Type
Human Otc Drug
FDA Application #
505G(a)(3)
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-15-2016
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 53125-817-29 identifies a specific commercial package of 1000 ml in 1 bag of North Woods Derma Foam E-2, a human over the counter drug labeled by Superior Chemical Corporation. This soap is formulated for topical use and contains benzalkonium 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 Superior Chemical Corporation on September 15, 2016. The current certification is valid through December 31, 2026.

How is this Superior Chemical Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 53125081729. 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)
53125-817-29
11-Digit CMS (5-4-2)
53125-0817-29

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