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  5. NDC Package Code: 47649-1201-2 Dr.whitiss 20%

NDC Package 47649-1201-2 Dr.whitiss 20%

Carbamide Peroxide Gel, Dentifrice Dental - 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:
47649-1201-2
Package Description:
4 SYRINGE in 1 PACKAGE / 1 g in 1 SYRINGE (47649-1201-1)
Product Code:
47649-1201
Proprietary Name:
Dr.whitiss 20%
Non-Proprietary Name:
Carbamide Peroxide
Substance Name:
Carbamide Peroxide
Usage Information:
This medication is used to treat earwax buildup. It helps to soften, loosen, and remove the earwax. Too much earwax can block the ear canal and reduce hearing. This medication releases oxygen and starts to foam when it comes in contact with the skin. The foaming helps break up and remove the earwax. Consult your doctor before using this product in children younger than 12 years.
11-Digit NDC Billing Format:
47649120102
NDC to RxNorm Crosswalk:
  • RxCUI: 1653117 - carbamide peroxide 20 % Oral Gel
  • RxCUI: 1653117 - carbamide peroxide 0.2 MG/MG Oral Gel
  • RxCUI: 1653117 - carbamide peroxide 20 % Dental Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Nibec Co., Ltd
    Dosage Form:
    Gel, Dentifrice - A combination of a dentifrice (formulation intended to clean and/or polish the teeth, and which may contain certain additional agents), and a gel. It is used with a toothbrush for the purpose of cleaning and polishing the teeth.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
    • Active Ingredient(s):
  • CARBAMIDE PEROXIDE 20 g/100g
    • Sample Package:
    No
    FDA Application Number:
    part356
    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:
    06-07-2015
    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 47649-1201-2?

    The NDC Packaged Code 47649-1201-2 is assigned to a package of 4 syringe in 1 package / 1 g in 1 syringe (47649-1201-1) of Dr.whitiss 20%, a human over the counter drug labeled by Nibec Co., Ltd. The product's dosage form is gel, dentifrice and is administered via dental form.

    Is NDC 47649-1201 included in the NDC Directory?

    Yes, Dr.whitiss 20% with product code 47649-1201 is active and included in the NDC Directory. The product was first marketed by Nibec Co., Ltd on June 07, 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 47649-1201-2?

    The 11-digit format is 47649120102. 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 5-4-1 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
    5-4-147649-1201-25-4-247649-1201-02