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  5. NDC Package Code: 50685-010-25 Bzk

NDC Package 50685-010-25 Bzk

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

Table of Contents

    1. Package Information
    2. 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:
50685-010-25
Package Description:
3 APPLICATOR in 1 BOX / 1 g in 1 APPLICATOR
Product Code:
50685-010
Proprietary Name:
Bzk
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Tear open pouch and use as part of your daily cleansing routine.Chean the affected area.Apply this product on the area 1 to 3 times daily.May be covered with a sterile bandage.If bandaged, let dry first.
11-Digit NDC Billing Format:
50685001025
NDC to RxNorm Crosswalk:
  • RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
  • RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
  • RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
  • RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Dalian Goodwood Medical Care Ltd.
    Dosage Form:
    Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
    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 mg/g
    • Sample Package:
    No
    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:
    03-19-2015
    End Marketing Date:
    04-30-2026
    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.

    Frequently Asked Questions

    What is NDC 50685-010-25?

    The NDC Packaged Code 50685-010-25 is assigned to a package of 3 applicator in 1 box / 1 g in 1 applicator of Bzk, a human over the counter drug labeled by Dalian Goodwood Medical Care Ltd.. The product's dosage form is swab and is administered via topical form.

    Is NDC 50685-010 included in the NDC Directory?

    Yes, Bzk with product code 50685-010 is active and included in the NDC Directory. The product was first marketed by Dalian Goodwood Medical Care Ltd. on March 19, 2015.

    What is the 11-digit format for NDC 50685-010-25?

    The 11-digit format is 50685001025. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-250685-010-255-4-250685-0010-25