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  5. NDC Package Code: 63783-500-04 Neutramaxx 5000 Plus Turbo

NDC Package 63783-500-04 Neutramaxx 5000 Plus Turbo

Sodium Fluoride Paste Oral - 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:
63783-500-04
Package Description:
112 g in 1 TUBE
Product Code:
63783-500
Proprietary Name:
Neutramaxx 5000 Plus Turbo
Non-Proprietary Name:
Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
INDICATIONS   NEUTRAMAXXtm 5000 PLUS TURBO IS A SELF-APPLIED DENTIFRICE FOR PREVENTION OF TOOTH DECAY, ORTHODONTIC DECALCIFICATION AND HYPERSENSITIVITY
11-Digit NDC Billing Format:
63783050004
NDC to RxNorm Crosswalk:
  • RxCUI: 1191716 - NeutraMaxx 500 Plus Turbo 1.1 % Dental Gel
  • RxCUI: 1191716 - sodium fluoride 0.011 MG/MG Toothpaste [Neutramaxx]
  • RxCUI: 1191716 - Neutramaxx 0.011 MG/MG Dental Gel
  • RxCUI: 1191716 - Neutramaxx 1.1 % Dental Gel
  • RxCUI: 392038 - sodium fluoride 1.1 % Toothpaste
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Massco Dental A Division Of Dunagin Pharmaceuticals
    Dosage Form:
    Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SODIUM FLUORIDE 1.1 g/112g
    • 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:
    09-01-2011
    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 63783-500-04?

    The NDC Packaged Code 63783-500-04 is assigned to a package of 112 g in 1 tube of Neutramaxx 5000 Plus Turbo, a human prescription drug labeled by Massco Dental A Division Of Dunagin Pharmaceuticals. The product's dosage form is paste and is administered via oral form.

    Is NDC 63783-500 included in the NDC Directory?

    Yes, Neutramaxx 5000 Plus Turbo with product code 63783-500 is active and included in the NDC Directory. The product was first marketed by Massco Dental A Division Of Dunagin Pharmaceuticals on September 01, 2011 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 63783-500-04?

    The 11-digit format is 63783050004. 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
    5-3-263783-500-045-4-263783-0500-04