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  5. NDC Package Code: 47649-1301-2 Dr.whitiss 35%

NDC Package 47649-1301-2 Dr.whitiss 35%

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
47649-1301-2
Package Description:
4 SYRINGE in 1 PACKAGE / 1 g in 1 SYRINGE (47649-1301-1)
Product Code:
47649-1301
Proprietary Name:
Dr.whitiss 35%
Usage Information:
1. Gingival and general oral heath should be confirmed before treatment.2. Brush your teeth before treatment.3. Follow your dentist’s instructions on how to load gel into your custom whitening tray. Use no more than 1/3 to 1/2 of the syringe per tray.4. Insert whitening tray in the mouth over the teeth. Seat the tray firmly agains the teeth. Remove excess gel with clean finger or soft toothbrush.(Rinse twice; do not swallow rinsed gel.)5. Unless directed otherwise by your dentist, wear Dr.Whitiss 10% for 8-10 hours or overnight, Dr.Whitiss 15% for 4-6 hours, Dr.Whitiss20% for 2-4 hours, and Dr.Whitiss 35% for 30 minutes.6. If significant sensitivity occurs, stop treatment and consult dentist.
11-Digit NDC Billing Format:
47649130102
Labeler Name:
Nibec Co., Ltd
Sample Package:
No
Start Marketing Date:
08-11-2015
Listing Expiration Date:
12-31-2023
Exclude Flag:
I
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 47649-1301-2?

The NDC Packaged Code 47649-1301-2 is assigned to a package of 4 syringe in 1 package / 1 g in 1 syringe (47649-1301-1) of Dr.whitiss 35%, labeled by Nibec Co., Ltd. The product's dosage form is and is administered via form.

Is NDC 47649-1301 included in the NDC Directory?

No, Dr.whitiss 35% with product code 47649-1301 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nibec Co., Ltd on August 11, 2015 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 47649-1301-2?

The 11-digit format is 47649130102. 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
5-4-147649-1301-25-4-247649-1301-02