NDC 71141-146 Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored

Natural Psyllium Husk Powder Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
71141-146
Proprietary Name:
Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored
Non-Proprietary Name: [1]
Natural Psyllium Husk
Substance Name: [2]
Psyllium Husk
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Lidl Us, Llc
    Labeler Code:
    71141
    FDA Application Number: [6]
    part334
    Marketing Category: [8]
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date: [9]
    11-15-2018
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    BROWN (C48332 - LIGHT YELLOWISH)
    Imprint(s):
    RP146
    Flavor(s):
    ORANGE (C73406 - NATURAL AND ARTIFCIAL)

    Product Packages

    NDC Code 71141-146-32

    Package Description: 660 g in 1 BOTTLE, PLASTIC

    Product Details

    What is NDC 71141-146?

    The NDC code 71141-146 is assigned by the FDA to the product Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored which is a human over the counter drug product labeled by Lidl Us, Llc. The generic name of Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored is natural psyllium husk. The product's dosage form is powder and is administered via oral form. The product is distributed in a single package with assigned NDC code 71141-146-32 660 g in 1 bottle, plastic . 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 Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored?

    This medication is used to treat constipation. It increases the bulk in your stool, an effect that helps to cause movement of the intestines. It also works by increasing the amount of water in the stool, making the stool softer and easier to pass. Psyllium, one type of bulk-forming laxative, has also been used along with a proper diet to treat high cholesterol.

    What are Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored 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.

    Which are Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored UNII Codes?

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

    Which are Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored 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 Lidl Orange Smooth Fiber Powder Sugar Free Naturally And Artificially Flavored?

    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

    Psyllium


    Psyllium, a bulk-forming laxative, is used to treat constipation. It absorbs liquid in the intestines, swells, and forms a bulky stool, which is easy to pass. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
    [Learn More]


    Black Psyllium


    What is it? Black psyllium comes from the seed husks of the Plantago arenaria plant. It contains high amounts of soluble dietary fiber.

    Black psyllium adds bulk to the stool which might help with constipation, diarrhea, and irritable bowel syndrome (IBS). It also controls how quickly sugars are absorbed from the gut, which might help control blood sugar levels in people with diabetes.

    People commonly use black psyllium for treating and preventing constipation. It is also used for diarrhea, obesity, diabetes, high blood pressure, and many other conditions, but there is no good scientific evidence to support most of these uses.

    Don't confuse black psyllium with blond psyllium. These are not the same.


    [Learn More]


    Blond Psyllium


    What is it? Blond psyllium (Plantago ovata) is an herb. Its seed husk is used as a laxative and stool softener and to help reduce cholesterol.

    Psyllium seed husks absorb water in the stomach and form a large mass. This mass stimulates the bowel in people with constipation. In people with diarrhea, it can slow down the bowel and reduce bowel movements. This mass can also reduce the amount of cholesterol that is absorbed into the body.

    Blond psyllium is commonly used as a stool softener in people with constipation and hemorrhoids. It is also used for diarrhea, irritable bowel syndrome (IBS), high cholesterol, heart disease, and diabetes. It's used for many other conditions, but there is no good scientific evidence to support most of these other 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".