NDC Package 81990-001-01 Hops Antibacterial Wet Wipes

Benzalkonium Chloride 0.10% 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:
81990-001-01
Package Description:
60 U in 1 POUCH
Product Code:
Proprietary Name:
Hops Antibacterial Wet Wipes
Non-Proprietary Name:
Benzalkonium Chloride 0.10%
Substance Name:
Benzalkonium Chloride
Usage Information:
Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.
11-Digit NDC Billing Format:
81990000101
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:
    Sapro Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi
    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:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-01-2021
    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 81990-001-01?

    The NDC Packaged Code 81990-001-01 is assigned to a package of 60 u in 1 pouch of Hops Antibacterial Wet Wipes, a human over the counter drug labeled by Sapro Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi. The product's dosage form is cloth and is administered via topical form.

    Is NDC 81990-001 included in the NDC Directory?

    Yes, Hops Antibacterial Wet Wipes with product code 81990-001 is active and included in the NDC Directory. The product was first marketed by Sapro Temizlik Urunleri Sanayi Ve Ticaret Anonim Sirketi on July 01, 2021 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 81990-001-01?

    The 11-digit format is 81990000101. 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
    5-3-281990-001-015-4-281990-0001-01