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  2. Glaxosmithkline Consumer Healthcare Holdings (us) Llc
  3. NDC Product Code: 0067-8140 Ex-lax Regular Strength Chocolated Stimulant Laxative

NDC 0067-8140 Ex-lax Regular Strength Chocolated Stimulant Laxative

Sennosides Tablet, Chewable Oral - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 0067-8140?
    5. Ex-lax Regular Strength Chocolated Stimulant Laxative Uses
    6. Active Ingredients
    7. Active Ingredients UNII Codes
    8. Inactive Ingredients UNII Codes
    9. NDC to RxNorm Crosswalk
    10. Patient Education

Product Information

NDC Product Code:
0067-8140
Proprietary Name:
Ex-lax Regular Strength Chocolated Stimulant Laxative
Non-Proprietary Name: [1]
Sennosides
Substance Name: [2]
Sennosides
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Glaxosmithkline Consumer Healthcare Holdings (us) Llc
    Labeler Code:
    0067
    Product Label ID:
    59a26a7f-516f-4507-8dec-f40cf6cfaffc
    FDA Application Number: [6]
    M007
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    08-01-2017
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    BROWN (C48332)
    Shape:
    RECTANGLE (C48347)
    Size(s):
    68 MM
    Imprint(s):
    EX;LAX
    Score:
    1
    Flavor(s):
    CHOCOLATE (C73376)

    Product Packages

    NDC Code 0067-8140-01

    Package Description: 1 PACKAGE in 1 BOX / 12 TABLET, CHEWABLE in 1 PACKAGE

    NDC Code 0067-8140-02

    Package Description: 2 PACKAGE in 1 BOX / 12 TABLET, CHEWABLE in 1 PACKAGE

    NDC Code 0067-8140-03

    Package Description: 4 PACKAGE in 1 BOX / 12 TABLET, CHEWABLE in 1 PACKAGE

    Product Details

    What is NDC 0067-8140?

    The NDC code 0067-8140 is assigned by the FDA to the product Ex-lax Regular Strength Chocolated Stimulant Laxative which is a human over the counter drug product labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The generic name of Ex-lax Regular Strength Chocolated Stimulant Laxative is sennosides. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in 3 packages with assigned NDC codes 0067-8140-01 1 package in 1 box / 12 tablet, chewable in 1 package, 0067-8140-02 2 package in 1 box / 12 tablet, chewable in 1 package, 0067-8140-03 4 package in 1 box / 12 tablet, chewable in 1 package. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Ex-lax Regular Strength Chocolated Stimulant Laxative?

    Sennosides are used to treat constipation. They may also be used to clean out the intestines before a bowel examination/surgery. Sennosides are known as stimulant laxatives. They work by keeping water in the intestines, which causes movement of the intestines.

    What are Ex-lax Regular Strength Chocolated Stimulant Laxative Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • SENNOSIDES 15 mg/1 - Medications derived from SENNA EXTRACT that are used to treat CONSTIPATION.

    Which are Ex-lax Regular Strength Chocolated Stimulant Laxative UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Ex-lax Regular Strength Chocolated Stimulant Laxative Inactive Ingredients UNII Codes?

    The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

    What is the NDC to RxNorm Crosswalk for Ex-lax Regular Strength Chocolated Stimulant Laxative?

    RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

    * Please review the disclaimer below.

    Patient Education

    Senna


    Senna is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Senna is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
    [Learn More]


    Senna


    What is it? Senna is the fruit (pod) or leaf of the plant Senna alexandrina. It is approved in the US as a laxative for short-term treatment of constipation.

    Senna contains many chemicals called sennosides. Sennosides irritate the lining of the bowel, which causes a laxative effect.

    Senna is an FDA-approved over-the-counter (OTC) laxative. It is used to treat constipation and also to clear the bowel before procedures such as colonoscopy. People also use senna for irritable bowel syndrome (IBS), hemorrhoids, weight loss, and many other conditions, but there is no good scientific evidence to support these uses.


    [Learn More]


    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

    [12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".