1. Home
  2. Labeler Index
  3. Kay Chemical Company
  4. 63146-111
  5. NDC Package Code: 63146-111-03 Qsr

NDC Package 63146-111-03 Qsr

Chloroxyenol 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:
63146-111-03
Package Description:
750 mL in 1 BOTTLE, PLASTIC
Product Code:
63146-111
Proprietary Name:
Qsr
Non-Proprietary Name:
Chloroxyenol
Substance Name:
Chloroxylenol
Usage Information:
Wet hands and forearms. • Apply palmful to hands and forearms. • Scrub Thoroughly. • Scrub thoroughly. • Rinse and dry.
11-Digit NDC Billing Format:
63146011103
NDC to RxNorm Crosswalk:
  • RxCUI: 1039003 - QSR Antibacterial 0.5 % Medicated Liquid Soap
  • RxCUI: 1039003 - chloroxylenol 5 MG/ML Medicated Liquid Soap [QSR Antibacterial]
  • RxCUI: 1039003 - QSR Antibacterial 5 MG/ML Medicated Liquid Soap
  • RxCUI: 436367 - chloroxylenol 0.5 % Medicated Liquid Soap
  • RxCUI: 436367 - chloroxylenol 5 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Kay Chemical 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):
  • CHLOROXYLENOL 5 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:
    02-22-2010
    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
    63146-111-101250 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63146-111-03?

    The NDC Packaged Code 63146-111-03 is assigned to a package of 750 ml in 1 bottle, plastic of Qsr, a human over the counter drug labeled by Kay Chemical Company. The product's dosage form is solution and is administered via topical form.

    Is NDC 63146-111 included in the NDC Directory?

    Yes, Qsr with product code 63146-111 is active and included in the NDC Directory. The product was first marketed by Kay Chemical Company on February 22, 2010 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 63146-111-03?

    The 11-digit format is 63146011103. 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
    5-3-263146-111-035-4-263146-0111-03