NDC Package 80337-701-01 Disinfect Wet Wipes

Benzalkonium Chloride Cloth 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:
80337-701-01
Package Description:
100 CLOTH in 1 CANISTER
Product Code:
Proprietary Name:
Disinfect Wet Wipes
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Wipe the surface of the skin and let it dry naturally.Supervise children under 6 years of age when using this product to avoid swallowing.
11-Digit NDC Billing Format:
80337070101
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 Xiaolikang Medical Technology Co., Ltd.
    Dosage Form:
    Cloth - A large piece of relatively flat, absorbent material that contains a drug. It 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:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-05-2020
    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 80337-701-01?

    The NDC Packaged Code 80337-701-01 is assigned to a package of 100 cloth in 1 canister of Disinfect Wet Wipes, a human over the counter drug labeled by Jiangsu Xiaolikang Medical Technology Co., Ltd.. The product's dosage form is cloth and is administered via topical form.

    Is NDC 80337-701 included in the NDC Directory?

    Yes, Disinfect Wet Wipes with product code 80337-701 is active and included in the NDC Directory. The product was first marketed by Jiangsu Xiaolikang Medical Technology Co., Ltd. on November 05, 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 80337-701-01?

    The 11-digit format is 80337070101. 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
    5-3-280337-701-015-4-280337-0701-01