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  5. NDC Package Code: 49354-055-75 X3 Clean Foaming Hand Sanitizer

NDC Package 49354-055-75 X3 Clean Foaming Hand Sanitizer

Benzalkonium Chloride Aerosol, Foam 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:
49354-055-75
Package Description:
75 mL in 1 BOTTLE, PUMP
Product Code:
49354-055
Proprietary Name:
X3 Clean Foaming Hand Sanitizer
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Apply a small amount to palms and rub hands thoroughly until completely dry.
11-Digit NDC Billing Format:
49354005575
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:
    Hk Kolmar Canada, Inc
    Dosage Form:
    Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
    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:
    05-01-2019
    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.

    Frequently Asked Questions

    What is NDC 49354-055-75?

    The NDC Packaged Code 49354-055-75 is assigned to a package of 75 ml in 1 bottle, pump of X3 Clean Foaming Hand Sanitizer, a human over the counter drug labeled by Hk Kolmar Canada, Inc. The product's dosage form is aerosol, foam and is administered via topical form.

    Is NDC 49354-055 included in the NDC Directory?

    Yes, X3 Clean Foaming Hand Sanitizer with product code 49354-055 is active and included in the NDC Directory. The product was first marketed by Hk Kolmar Canada, Inc on May 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 49354-055-75?

    The 11-digit format is 49354005575. 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
    5-3-249354-055-755-4-249354-0055-75