NDC Package 79531-003-01 Multi-purpose Antibacterial 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:
79531-003-01
Package Description:
77 g in 1 BAG
Product Code:
Proprietary Name:
Multi-purpose Antibacterial Wet Wipes
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.
11-Digit NDC Billing Format:
79531000301
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:
    Supreme Premium Products,inc.
    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:
    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:
    07-11-2020
    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.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    79531-003-02295 g in 1 BAG
    79531-003-03435 g in 1 PAIL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 79531-003-01?

    The NDC Packaged Code 79531-003-01 is assigned to a package of 77 g in 1 bag of Multi-purpose Antibacterial Wet Wipes, a human over the counter drug labeled by Supreme Premium Products,inc.. The product's dosage form is cloth and is administered via topical form.

    Is NDC 79531-003 included in the NDC Directory?

    Yes, Multi-purpose Antibacterial Wet Wipes with product code 79531-003 is active and included in the NDC Directory. The product was first marketed by Supreme Premium Products,inc. on July 11, 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 79531-003-01?

    The 11-digit format is 79531000301. 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
    5-3-279531-003-015-4-279531-0003-01