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NDC 83027-0048 Industriox

Berberis Vulgaris,Taraxacum Officinale,Ammonium Carbonicum,Camphora,Spinacia,Sulphuricum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83027-0048?
  4. Industriox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
83027-0048
Proprietary Name:
Industriox
Non-Proprietary Name: [1]
Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum, Camphora, Spinacia, Sulphuricum Acidum, Nux Vomica, Acetone, Benzinum, Butyl Methacrylate, Calcarea Carbonica, Lachesis Mutus, Methyl Ethyl Ketone, Naphthalinum, Plumbum Metallicum, Trichloroethylene, Forlmalinum, Mtbe (tert-butyl Methyl Ether), Petroleum, Carboneum Chloratum
Substance Name: [2]
Acetone; Ammonium Carbonate; Benzene; Berberis Vulgaris Root Bark; Camphor (natural); Carbon Tetrachloride; Formaldehyde Solution; Kerosene; Lachesis Muta Venom; Lead; Methyl Ethyl Ketone; N-butyl Methacrylate; Naphthalene; Oyster Shell Calcium Carbonate, Crude; Spinacia Oleracea Root; Strychnos Nux-vomica Seed; Sulfuric Acid; Taraxacum Officinale; Tert-butyl Methyl Ether; Trichloroethylene
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Nutritional Specialties, Inc.
    Labeler Code:
    83027
    Product Label ID:
    d77a58f8-68c3-4772-b938-473b203a1d47
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-25-2023
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 83027-0048?

    The NDC code 83027-0048 is assigned by the FDA to the product Industriox which is a human over the counter drug product labeled by Nutritional Specialties, Inc.. The generic name of Industriox is berberis vulgaris, taraxacum officinale, ammonium carbonicum, camphora, spinacia, sulphuricum acidum, nux vomica, acetone, benzinum, butyl methacrylate, calcarea carbonica, lachesis mutus, methyl ethyl ketone, naphthalinum, plumbum metallicum, trichloroethylene, forlmalinum, mtbe (tert-butyl methyl ether), petroleum, carboneum chloratum. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 83027-0048-1 60 ml in 1 bottle, spray . 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 Industriox?

    Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. For highly sensitive individuals: best tolerated administration is through imbrication (RUBBING IN) on skin at pulse points or abdomen. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

    What are Industriox 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 Industriox UNII Codes?

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

    Which are Industriox 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:

    Which are the Pharmacologic Classes for Industriox?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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    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.

    [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".