NDC Package 76402-405-03 Juniper Breeze Foaming Antimicrobial

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

Package Information
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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:

76402-405-03

Package Description:

4 BOTTLE, PLASTIC in 1 CARTON / 1250 mL in 1 BOTTLE, PLASTIC

Product Code:

76402-405

Proprietary Name:

Juniper Breeze Foaming Antimicrobial

Non-Proprietary Name:

Benzalkonium Chloride

Substance Name:

Benzalkonium Chloride

Usage Information:

•Apply soap to palm of hand.•Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds.•Rinse with water until all soap is removed from hands.•Dry completely (incomplete drying may lead to chapped skin).•Children under 6 years of age should be supervised when using this product.

11-Digit NDC Billing Format:

76402040503

NDC to RxNorm Crosswalk:

RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap

RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap

RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap

Product Type:

Human Otc Drug

Labeler Name:

Hillyard Gmp

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.

Active Ingredient(s):

BENZALKONIUM CHLORIDE .13 g/100mL

Sample Package:

FDA Application Number:

M003

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

03-01-2020

End Marketing Date:

06-01-2024

Exclude Flag:

Code Structure:

76402 - Hillyard Gmp
- 76402-405 - Juniper Breeze Foaming Antimicrobial
  - 76402-405-03 - 4 BOTTLE, PLASTIC in 1 CARTON / 1250 mL in 1 BOTTLE, PLASTIC

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
76402-405-02	3 BOTTLE, PLASTIC in 1 CARTON / 1000 mL in 1 BOTTLE, PLASTIC
76402-405-06	4 BOTTLE, PLASTIC in 1 CARTON / 3785 mL in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 76402-405-03?

The NDC Packaged Code 76402-405-03 is assigned to a package of 4 bottle, plastic in 1 carton / 1250 ml in 1 bottle, plastic of Juniper Breeze Foaming Antimicrobial, a human over the counter drug labeled by Hillyard Gmp. The product's dosage form is liquid and is administered via topical form.

Is NDC 76402-405 included in the NDC Directory?

Yes, Juniper Breeze Foaming Antimicrobial with product code 76402-405 is active and included in the NDC Directory. The product was first marketed by Hillyard Gmp on March 01, 2020.

What is the 11-digit format for NDC 76402-405-03?

The 11-digit format is 76402040503. 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	76402-405-03	5-4-2	76402-0405-03

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