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  5. NDC Package Code: 73656-007-00 White Glo Professional Choice

NDC Package 73656-007-00 White Glo Professional Choice

Sodium Monofluorophosphate Kit - 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:
73656-007-00
Package Description:
1 KIT in 1 KIT * 150 g in 1 TUBE (73656-008-00)
Product Code:
73656-007
Proprietary Name:
White Glo Professional Choice
Non-Proprietary Name:
Sodium Monofluorophosphate
Usage Information:
Adults and children 2 years of age & older:  Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age: Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.Children under 2 years of age: Consult a dentist or doctor.
11-Digit NDC Billing Format:
73656000700
NDC to RxNorm Crosswalk:
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste
    • Product Type:
    Human Otc Drug
    Labeler Name:
    White Glo Usa Inc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    M021
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    02-15-2020
    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 73656-007-00?

    The NDC Packaged Code 73656-007-00 is assigned to a package of 1 kit in 1 kit * 150 g in 1 tube (73656-008-00) of White Glo Professional Choice, a human over the counter drug labeled by White Glo Usa Inc. The product's dosage form is kit and is administered via form.

    Is NDC 73656-007 included in the NDC Directory?

    Yes, White Glo Professional Choice with product code 73656-007 is active and included in the NDC Directory. The product was first marketed by White Glo Usa Inc on February 15, 2020 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 73656-007-00?

    The 11-digit format is 73656000700. 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
    5-3-273656-007-005-4-273656-0007-00