NDC Package 41250-739-01 Stool Softener Plus Stimulant Laxative

Docusate Sodium,Sennosides Tablet Oral - 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:
41250-739-01
Package Description:
1 BOTTLE in 1 PACKAGE / 100 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Stool Softener Plus Stimulant Laxative
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:
41250073901
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:
Meijer Distribution 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.
Sample Package:
No
FDA Application Number:
M007
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-07-2020
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 41250-739-01?

The NDC Packaged Code 41250-739-01 is assigned to a package of 1 bottle in 1 package / 100 tablet in 1 bottle of Stool Softener Plus Stimulant Laxative, a human over the counter drug labeled by Meijer Distribution Inc.. The product's dosage form is tablet and is administered via oral form.

Is NDC 41250-739 included in the NDC Directory?

Yes, Stool Softener Plus Stimulant Laxative with product code 41250-739 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution Inc. on April 07, 2020 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 41250-739-01?

The 11-digit format is 41250073901. 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
5-3-241250-739-015-4-241250-0739-01