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NDC 66096-706 Ohm Mucus Relief

Antimonium Crudum,Antimonium Tartaricum,Chelidonium Majus,Ferrum Phosphoricum,Kali - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66096-706?
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
66096-706
Proprietary Name:
Ohm Mucus Relief
Non-Proprietary Name: [1]
Antimonium Crudum, Antimonium Tartaricum, Chelidonium Majus, Ferrum Phosphoricum, Kali Carboonicum, Kali Muriaticum, Kali Sulphuricum, Marrubium Vulgare.
Substance Name: [2]
Antimony Potassium Tartrate; Antimony Trisulfide; Chelidonium Majus; Ferrosoferric Phosphate; Marrubium Vulgare; Potassium Carbonate; Potassium Chloride; Potassium Dichromate; Potassium Sulfate
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]
    Ohm Pharma Inc.
    Labeler Code:
    66096
    Product Label ID:
    f13bff50-7087-46dc-a958-b460a2af6283
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    05-14-2015
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    Size(s):
    6 MM
    Score:
    1

    Code Structure Chart

    Product Details

    What is NDC 66096-706?

    The NDC code 66096-706 is assigned by the FDA to the product Ohm Mucus Relief which is a human over the counter drug product labeled by Ohm Pharma Inc.. The generic name of Ohm Mucus Relief is antimonium crudum, antimonium tartaricum, chelidonium majus, ferrum phosphoricum, kali carboonicum, kali muriaticum, kali sulphuricum, marrubium vulgare.. The product's dosage form is tablet, chewable and is administered via oral form. The product is distributed in a single package with assigned NDC code 66096-706-23 186 tablet, chewable in 1 bottle . 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 Ohm Mucus Relief 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.
    • ANTIMONY POTASSIUM TARTRATE 6 [hp_C]/1 - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
    • ANTIMONY TRISULFIDE 6 [hp_C]/1
    • CHELIDONIUM MAJUS 6 [hp_X]/1 - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
    • FERROSOFERRIC PHOSPHATE 6 [hp_X]/1
    • MARRUBIUM VULGARE 9 [hp_C]/1 - A plant genus of the LAMIACEAE family that contains marrubiin (a labdane diterpene). It is known as a traditional medicinal for sore throat.
    • POTASSIUM CARBONATE 30 [hp_C]/1
    • POTASSIUM CHLORIDE 6 [hp_X]/1 - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
    • POTASSIUM DICHROMATE 12 [hp_X]/1 - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
    • POTASSIUM SULFATE 6 [hp_X]/1

    Which are Ohm Mucus Relief UNII Codes?

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

    Which are Ohm Mucus Relief 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 Ohm Mucus Relief?

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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".