NDC Package 53125-700-57 North Woods Derma Foam Hand Sanitizer

Benzalkonium Chloride Soap Topical - View Billable Units, 11-Digit Format, RxNorm

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Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:

53125-700-57

Package Description:

550 mL in 1 BOTTLE, PUMP

Product Code:

53125-700

Proprietary Name:

North Woods Derma Foam Hand Sanitizer

Non-Proprietary Name:

Benzalkonium Chloride

Substance Name:

Benzalkonium Chloride

Usage Information:

UsesUse in a variety of public facilities.Use this product when soap and water are not available.

11-Digit NDC Billing Format:

53125070057

NDC to RxNorm Crosswalk:

RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam

RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam

Product Type:

Human Otc Drug

Labeler Name:

Superior Chemical Corporation

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(s):

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

Sample Package:

FDA Application Number:

part333A

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:

10-01-2015

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

53125 - Superior Chemical Corporation
- 53125-700 - North Woods Derma Foam Hand Sanitizer
  - 53125-700-57 - 550 mL in 1 BOTTLE, PUMP

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 disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
53125-700-54	1000 mL in 1 BAG
53125-700-88	500 mL in 1 BOTTLE, PUMP

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 53125-700-57?

The NDC Packaged Code 53125-700-57 is assigned to a package of 550 ml in 1 bottle, pump of North Woods Derma Foam Hand Sanitizer, a human over the counter drug labeled by Superior Chemical Corporation. The product's dosage form is soap and is administered via topical form.

Is NDC 53125-700 included in the NDC Directory?

Yes, North Woods Derma Foam Hand Sanitizer with product code 53125-700 is active and included in the NDC Directory. The product was first marketed by Superior Chemical Corporation on October 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 53125-700-57?

The 11-digit format is 53125070057. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	53125-700-57	5-4-2	53125-0700-57

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