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  5. NDC Package Code: 50814-057-01 Genuine First Aid Antiseptic Towelette

NDC Package 50814-057-01 Genuine First Aid Antiseptic Towelette

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:
50814-057-01
Package Description:
1 PACKAGE in 1 BAG / .225 mL in 1 PACKAGE
Product Code:
50814-057
Proprietary Name:
Genuine First Aid Antiseptic Towelette
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
11-Digit NDC Billing Format:
50814005701
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:
    Gfa Production (xiamen) 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):
  • BENZALKONIUM CHLORIDE 1.3 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-2020
    Listing Expiration Date:
    12-31-2024
    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 50814-057-01?

    The NDC Packaged Code 50814-057-01 is assigned to a package of 1 package in 1 bag / .225 ml in 1 package of Genuine First Aid Antiseptic Towelette, a human over the counter drug labeled by Gfa Production (xiamen) Co., Ltd.. The product's dosage form is swab and is administered via topical form.

    Is NDC 50814-057 included in the NDC Directory?

    Yes, Genuine First Aid Antiseptic Towelette with product code 50814-057 is active and included in the NDC Directory. The product was first marketed by Gfa Production (xiamen) Co., Ltd. on January 01, 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 50814-057-01?

    The 11-digit format is 50814005701. 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
    5-3-250814-057-015-4-250814-0057-01