NDC Package 50865-688-09 Ezfoam Foaming Alcohol Hand Sanitizer

Foaming Hand Sanitizer Solution 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:
50865-688-09
Package Description:
3785 mL in 1 JUG
Product Code:
Proprietary Name:
Ezfoam Foaming Alcohol Hand Sanitizer
Non-Proprietary Name:
Foaming Hand Sanitizer
Substance Name:
Alcohol
Usage Information:
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.Avoid contact with eyes. If eye contact occurs, flush with water.Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.Keep out of reach of children. If swallowed, contact a physician or poison control center.
11-Digit NDC Billing Format:
50865068809
NDC to RxNorm Crosswalk:
  • RxCUI: 616763 - ethanol 62 % Topical Foam
  • RxCUI: 616763 - ethanol 0.62 ML/ML Topical Foam
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Kutol Products Company
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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:
    06-27-2013
    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
    50865-688-1750 mL in 1 BOTTLE, PLASTIC
    50865-688-241000 mL in 1 BAG
    50865-688-411000 mL in 1 BAG
    50865-688-501200 mL in 1 BAG
    50865-688-78950 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50865-688-09?

    The NDC Packaged Code 50865-688-09 is assigned to a package of 3785 ml in 1 jug of Ezfoam Foaming Alcohol Hand Sanitizer, a human over the counter drug labeled by Kutol Products Company. The product's dosage form is solution and is administered via topical form.

    Is NDC 50865-688 included in the NDC Directory?

    Yes, Ezfoam Foaming Alcohol Hand Sanitizer with product code 50865-688 is active and included in the NDC Directory. The product was first marketed by Kutol Products Company on June 27, 2013 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 50865-688-09?

    The 11-digit format is 50865068809. 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
    5-3-250865-688-095-4-250865-0688-09