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  4. NDC Product Code: 53590-100 Mozi-q

NDC 53590-100 Mozi-q

Ledum Palustre Twig,Urtica Urens,Simaba Cedron Seed,Delphinium Staphisagria Seed,Grindelia - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 53590-100?
  5. Mozi-q Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
53590-100
Proprietary Name:
Mozi-q
Non-Proprietary Name: [1]
Ledum Palustre Twig, Urtica Urens, Simaba Cedron Seed, Delphinium Staphisagria Seed, Grindelia Hirsutula Flowering Top
Substance Name: [2]
Delphinium Staphisagria Seed; Grindelia Hirsutula Flowering Top; Ledum Palustre Twig; Simaba Cedron Seed; Urtica Urens
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]
    Xerion Dispensary Ltd.
    Labeler Code:
    53590
    Product Label ID:
    63e62403-b45c-46c1-9c41-639c673d8204
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-15-2012
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

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

    Code Structure Chart

    Product Details

    What is NDC 53590-100?

    The NDC code 53590-100 is assigned by the FDA to the product Mozi-q which is a human over the counter drug product labeled by Xerion Dispensary Ltd.. The generic name of Mozi-q is ledum palustre twig, urtica urens, simaba cedron seed, delphinium staphisagria seed, grindelia hirsutula flowering top. 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 53590-100-10 10 tablet, chewable in 1 box , 53590-100-30 30 tablet, chewable in 1 box , 53590-100-60 60 tablet, chewable in 1 box . 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 Mozi-q?

    Adults chew 1 tablet daily, or every 2-3 hours before going outside or when bug bites are present, up to a maximum of 8 tablets daily, or as directed by a health care practitioner. For best results, take between meals.

    What are Mozi-q 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 Mozi-q UNII Codes?

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

    • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
    • LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
    • URTICA URENS (UNII: IHN2NQ5OF9)
    • URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
    • SIMABA CEDRON SEED (UNII: KHI40967MV)
    • SIMABA CEDRON SEED (UNII: KHI40967MV) (Active Moiety)
    • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
    • DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
    • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI)
    • GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (Active Moiety)

    Which are Mozi-q 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:

    * 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.

    [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".