NDC Package 52261-0500-2 Berberex Wound Cleanser

Benzethonium Chloride Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

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:
52261-0500-2
Package Description:
237 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Berberex Wound Cleanser
Non-Proprietary Name:
Benzethonium Chloride
Substance Name:
Allantoin; Benzethonium Chloride
Usage Information:
Adults and children 2 years of age and older:use to clean minor cut, scrapes, and burns by thoroughly flushing the affected area let air drycover with adhesive bandage or sterile gauzeapply a small amount of this product on the area 1 to 3 times dailyChildren under 2 years of age:  do not use, consult a doctor
11-Digit NDC Billing Format:
52261050002
NDC to RxNorm Crosswalk:
  • RxCUI: 1437628 - allantoin 0.5 % / benzethonium chloride 0.1 % Topical Solution
  • RxCUI: 1437628 - allantoin 5 MG/ML / benzethonium chloride 1 MG/ML Topical Solution
  • RxCUI: 1487627 - BerbereX Wound Cleanser 0.5 % / 0.1 % Topical Solution
  • RxCUI: 1487627 - allantoin 5 MG/ML / benzethonium chloride 1 MG/ML Topical Solution [Berberex Wound Cleanser]
  • RxCUI: 1487627 - Berberex Wound Cleanser (allantoin 0.5 % / benzethonium chloride 0.1 % ) Topical Solution
Product Type:
Human Otc Drug
Labeler Name:
Cosco International, Inc.
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(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.
Sample Package:
No
FDA Application Number:
M003
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-17-2015
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 CodePackage Description
52261-0500-1118 mL in 1 BOTTLE, SPRAY
52261-0500-3473 mL in 1 BOTTLE, SPRAY

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 52261-0500-2?

The NDC Packaged Code 52261-0500-2 is assigned to a package of 237 ml in 1 bottle, spray of Berberex Wound Cleanser, a human over the counter drug labeled by Cosco International, Inc.. The product's dosage form is liquid and is administered via topical form.

Is NDC 52261-0500 included in the NDC Directory?

Yes, Berberex Wound Cleanser with product code 52261-0500 is active and included in the NDC Directory. The product was first marketed by Cosco International, Inc. on May 17, 2015 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 52261-0500-2?

The 11-digit format is 52261050002. 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 5-4-1 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-152261-0500-25-4-252261-0500-02