NDC Package 37808-549-29 Stool Softener And 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:
37808-549-29
Package Description:
240 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Stool Softener And 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 older take 2-4 tablets dailychildren 6 to under 12 years of age take 1-2 tablets dailychildren 2 to under 6 years of age take up to 1 tablet dailychildren under 2 years ask a doctor
11-Digit NDC Billing Format:
37808054929
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:
    H-e-b
    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:
    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:
    02-04-2022
    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 37808-549-29?

    The NDC Packaged Code 37808-549-29 is assigned to a package of 240 tablet in 1 bottle of Stool Softener And Stimulant Laxative, a human over the counter drug labeled by H-e-b. The product's dosage form is tablet and is administered via oral form.

    Is NDC 37808-549 included in the NDC Directory?

    Yes, Stool Softener And Stimulant Laxative with product code 37808-549 is active and included in the NDC Directory. The product was first marketed by H-e-b on February 04, 2022 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 37808-549-29?

    The 11-digit format is 37808054929. 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
    5-3-237808-549-295-4-237808-0549-29