NDC Package 69842-584-01 Cvs Foaming Hand Sanitizer Antibacterial

Benzalkonium Chloride Liquid 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:
69842-584-01
Package Description:
222 mL in 1 BOTTLE, DISPENSING
Product Code:
Proprietary Name:
Cvs Foaming Hand Sanitizer Antibacterial
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
♦place enough product in your palm to thoroughly cover your hands♦rub hands together briskly until dry ♦children under 6 years of age should be supervised when using this product
11-Digit NDC Billing Format:
69842058401
NDC to RxNorm Crosswalk:
  • RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam
  • RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Cvs Health
    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):
    Sample Package:
    No
    FDA Application Number:
    part333E
    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:
    01-01-2015
    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 69842-584-01?

    The NDC Packaged Code 69842-584-01 is assigned to a package of 222 ml in 1 bottle, dispensing of Cvs Foaming Hand Sanitizer Antibacterial, a human over the counter drug labeled by Cvs Health. The product's dosage form is liquid and is administered via topical form.

    Is NDC 69842-584 included in the NDC Directory?

    Yes, Cvs Foaming Hand Sanitizer Antibacterial with product code 69842-584 is active and included in the NDC Directory. The product was first marketed by Cvs Health on January 01, 2015 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 69842-584-01?

    The 11-digit format is 69842058401. 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
    5-3-269842-584-015-4-269842-0584-01