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  5. NDC Package Code: 50804-829-10 Stimulant Laxative Plus Stool Softener

NDC Package 50804-829-10 Stimulant Laxative Plus Stool Softener

Docusate Sodium,Sennosides Tablet 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:
50804-829-10
Package Description:
100 TABLET in 1 BOTTLE, PLASTIC
Product Code:
50804-829
Proprietary Name:
Stimulant Laxative Plus Stool Softener
Non-Proprietary Name:
Docusate Sodium, Sennosides
Substance Name:
Docusate Sodium; Sennosides
Usage Information:
Take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses. adults and children 12 years and over take 2-4 tablets daily children 6 to under 12 years of age take 1-2 tablets daily children 2 to under 6 years of age take up to 1 tablet daily children under 2 ask a doctor
11-Digit NDC Billing Format:
50804082910
NDC to RxNorm Crosswalk:
  • RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet
  • RxCUI: 998740 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
  • RxCUI: 998740 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Good Sense (geiss, Destin & Dunn, Inc.)
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DOCUSATE SODIUM 50 mg/1
  • SENNOSIDES 8.6 mg/1
    • Sample Package:
    No
    FDA Application Number:
    part334
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    12-31-2018
    End Marketing 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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50804-829-10?

    The NDC Packaged Code 50804-829-10 is assigned to a package of 100 tablet in 1 bottle, plastic of Stimulant Laxative Plus Stool Softener, a human over the counter drug labeled by Good Sense (geiss, Destin & Dunn, Inc.). The product's dosage form is tablet and is administered via oral form.

    Is NDC 50804-829 included in the NDC Directory?

    Yes, Stimulant Laxative Plus Stool Softener with product code 50804-829 is active and included in the NDC Directory. The product was first marketed by Good Sense (geiss, Destin & Dunn, Inc.) on December 31, 2018.

    What is the 11-digit format for NDC 50804-829-10?

    The 11-digit format is 50804082910. 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
    5-3-250804-829-105-4-250804-0829-10