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  5. NDC Package Code: 73927-0008-1 Nobaton 1% Alpha Hydroxy Acid Ampoule

NDC Package 73927-0008-1 Nobaton 1% Alpha Hydroxy Acid Ampoule

Nobaton 1% Alpha Hydroxy Acid Ampoule Toothpaste Ointment 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:
73927-0008-1
Package Description:
35 g in 1 TUBE
Product Code:
73927-0008
Proprietary Name:
Nobaton 1% Alpha Hydroxy Acid Ampoule
Non-Proprietary Name:
Nobaton 1% Alpha Hydroxy Acid Ampoule Toothpaste
Substance Name:
Olaflur; Sodium Monofluorophosphate
Usage Information:
Squeeze an appropriate amount of toothpaste onto the toothbrush, and brush teeth from the inside to the outside using an up and down rubbing motion. Rinse mouth after 3 minutes. (It is recommended to brush without water)
11-Digit NDC Billing Format:
73927000801
Product Type:
Human Otc Drug
Labeler Name:
Bd Technology Co.,ltd
Dosage Form:
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Dental - Administration to a tooth or teeth.
Active Ingredient(s):
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
04-21-2025
Listing Expiration Date:
12-31-2026
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 73927-0008-1?

The NDC Packaged Code 73927-0008-1 is assigned to a package of 35 g in 1 tube of Nobaton 1% Alpha Hydroxy Acid Ampoule, a human over the counter drug labeled by Bd Technology Co.,ltd. The product's dosage form is ointment and is administered via dental form.

Is NDC 73927-0008 included in the NDC Directory?

Yes, Nobaton 1% Alpha Hydroxy Acid Ampoule with product code 73927-0008 is active and included in the NDC Directory. The product was first marketed by Bd Technology Co.,ltd on April 21, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 73927-0008-1?

The 11-digit format is 73927000801. 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
5-4-173927-0008-15-4-273927-0008-01