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  5. NDC Package Code: 78691-023-00 Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent

NDC Package 78691-023-00 Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent

Benzalkonium Chloride Liquid 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:
78691-023-00
Package Description:
40 PATCH in 1 POUCH / 3.8 mL in 1 PATCH
Product Code:
78691-023
Proprietary Name:
Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Apply to hands, allow to air dry without wiping.Children under 6 years of age should be supervised when using this product. 
11-Digit NDC Billing Format:
78691002300
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:
    Quest Usa Corp
    Dosage Form:
    Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
    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:
    08-07-2023
    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 78691-023-00?

    The NDC Packaged Code 78691-023-00 is assigned to a package of 40 patch in 1 pouch / 3.8 ml in 1 patch of Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent, a human over the counter drug labeled by Quest Usa Corp. The product's dosage form is liquid and is administered via topical form.

    Is NDC 78691-023 included in the NDC Directory?

    Yes, Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent with product code 78691-023 is active and included in the NDC Directory. The product was first marketed by Quest Usa Corp on August 07, 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 78691-023-00?

    The 11-digit format is 78691002300. 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
    5-3-278691-023-005-4-278691-0023-00