NDC Package 80514-003-01 Bzk Antiseptic Swab

Benzalkonium Chloride Swab 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:
80514-003-01
Package Description:
.5 g in 1 POUCH
Product Code:
Proprietary Name:
Bzk Antiseptic Swab
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Clean the affected area.Apply a small amount of 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:
80514000301
NDC to RxNorm Crosswalk:
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Jiangsu Haida International Trading Co., 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):
    Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-04-2020
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

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    Frequently Asked Questions

    What is NDC 80514-003-01?

    The NDC Packaged Code 80514-003-01 is assigned to a package of .5 g in 1 pouch of Bzk Antiseptic Swab, a human over the counter drug labeled by Jiangsu Haida International Trading Co., Ltd.. The product's dosage form is swab and is administered via topical form.

    Is NDC 80514-003 included in the NDC Directory?

    Yes, Bzk Antiseptic Swab with product code 80514-003 is active and included in the NDC Directory. The product was first marketed by Jiangsu Haida International Trading Co., Ltd. on September 04, 2020 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 80514-003-01?

    The 11-digit format is 80514000301. 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
    5-3-280514-003-015-4-280514-0003-01