NDC Package 84727-051-01 Whitening

Yayashi Whitening Gel, Dentifrice Dental - View Billable Units, 11-Digit Format, RxNorm

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:
84727-051-01
Package Description:
100 g in 1 TUBE
Product Code:
Proprietary Name:
Whitening
Non-Proprietary Name:
Yayashi Whitening
Substance Name:
Glycerin; Hydrated Silica; Xanthan Gum
Usage Information:
Indications:This product is intended for individuals looking to remove surface stains and achieve a natural whitening effect. Suitable for adults experiencing mild tooth discoloration caused by coffee, tea, red wine, or smoking. Not recommended for individuals with sensitive teeth or gums. Please consult a dentist before use if you have dental concerns. Usage:Use twice daily, morning and night. Apply a pea-sized amount of toothpaste to your toothbrush. Gently brush teeth for at least two minutes, ensuring the toothpaste covers all tooth surfaces. Rinse thoroughly after brushing; avoid swallowing. For optimal whitening results, continue use for at least two weeks, and limit consumption of stain-causing foods and drinks.
11-Digit NDC Billing Format:
84727005101
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Baishili Trading 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.
Sample Package:
No
FDA Application Number:
M022
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
11-01-2024
Listing Expiration Date:
12-31-2025
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.

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Frequently Asked Questions

What is NDC 84727-051-01?

The NDC Packaged Code 84727-051-01 is assigned to a package of 100 g in 1 tube of Whitening, a human over the counter drug labeled by Guangzhou Baishili Trading Co., Ltd. The product's dosage form is gel, dentifrice and is administered via dental form.

Is NDC 84727-051 included in the NDC Directory?

Yes, Whitening with product code 84727-051 is active and included in the NDC Directory. The product was first marketed by Guangzhou Baishili Trading Co., Ltd on November 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 84727-051-01?

The 11-digit format is 84727005101. 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
5-3-284727-051-015-4-284727-0051-01