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  5. NDC Package Code: 63998-764-01 Alcohol-free Hand Sanitizing Foam

NDC Package 63998-764-01 Alcohol-free Hand Sanitizing Foam

Benzalkonium Chloride Solution Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
63998-764-01
Package Description:
59 mL in 1 BOTTLE
Product Code:
63998-764
Proprietary Name:
Alcohol-free Hand Sanitizing Foam
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.
11-Digit NDC Billing Format:
63998076401
NDC to RxNorm Crosswalk:
  • RxCUI: 1038799 - benzalkonium chloride 0.1 % Topical Foam
  • RxCUI: 1038799 - benzalkonium chloride 1 MG/ML Topical Foam
    • Product Type:
    Human Otc Drug
    Labeler Name:
    United Laboratories Inc.
    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):
  • BENZALKONIUM CHLORIDE 1 mg/mL
    • 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:
    01-01-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63998-764-02750 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63998-764-01?

    The NDC Packaged Code 63998-764-01 is assigned to a package of 59 ml in 1 bottle of Alcohol-free Hand Sanitizing Foam, a human over the counter drug labeled by United Laboratories Inc.. The product's dosage form is solution and is administered via topical form.

    Is NDC 63998-764 included in the NDC Directory?

    Yes, Alcohol-free Hand Sanitizing Foam with product code 63998-764 is active and included in the NDC Directory. The product was first marketed by United Laboratories Inc. on January 01, 2019 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 63998-764-01?

    The 11-digit format is 63998076401. 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
    5-3-263998-764-015-4-263998-0764-01