NDC Package 78564-006-10 Wet Wipes Ten

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:
78564-006-10
Package Description:
100 CLOTH in 1 POUCH
Product Code:
Proprietary Name:
Wet Wipes Ten
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Do not expose to direct sunlight, preferably place them in a cool place. Do not use on furniture. Do not flush down toilets. dispose in trash receptacles.Remove lid and open the seal. Pull up the conrer of the center sheet, twist it and thread through the dispenser split in the lid. Pull sheet out at an angle. When finished close lid flap to retain moisture. Peel back flap on front to pull out a wipe.Unfold and wipe hands thoroughly.Reseal and let hands dry.No need to rinse.
11-Digit NDC Billing Format:
78564000610
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:
    Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama 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:
    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:
    06-01-2023
    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 78564-006-10?

    The NDC Packaged Code 78564-006-10 is assigned to a package of 100 cloth in 1 pouch of Wet Wipes Ten, a human over the counter drug labeled by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Anonim Sirketi. The product's dosage form is cloth and is administered via topical form.

    Is NDC 78564-006 included in the NDC Directory?

    Yes, Wet Wipes Ten with product code 78564-006 is active and included in the NDC Directory. The product was first marketed by Taha Kimya Kozmetik Ve Tuketim Urunleri Sanayi Pazarlama Anonim Sirketi on June 01, 2023 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 78564-006-10?

    The 11-digit format is 78564000610. 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
    5-3-278564-006-105-4-278564-0006-10