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  4. NDC Product Code: 34666-020 Arnica Treatment Pack

NDC 34666-020 Arnica Treatment Pack

Kit Oral; Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 34666-020?
  5. Arnica Treatment Pack Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
34666-020
Proprietary Name:
Arnica Treatment Pack
Non-Proprietary Name: [1]
Arnica Treatment Pack
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Nartex Laboratorios Homeopaticos Sa De Cv
    Labeler Code:
    34666
    Product Label ID:
    86431a9a-5b53-c28a-e053-2991aa0a9901
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    04-11-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325 - WHITE)
    WHITE (C48325)
    Shape:
    ROUND (C48348)
    FREEFORM (C48340)
    Size(s):
    10 MM
    Imprint(s):
    NONE

    Product Packages

    NDC Code 34666-020-01

    Package Description: 1 KIT in 1 KIT * 1 TABLET in 1 BOX

    Product Details

    What is NDC 34666-020?

    The NDC code 34666-020 is assigned by the FDA to the product Arnica Treatment Pack which is a human over the counter drug product labeled by Nartex Laboratorios Homeopaticos Sa De Cv. The product's dosage form is kit and is administered via oral; topical form. The product is distributed in a single package with assigned NDC code 34666-020-01 1 kit in 1 kit * 1 tablet 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 Arnica Treatment Pack?

    Adults and children 4 yers of age and older: take 2 tablets every 6 hours, slowly dissolving in the mouthChildren under 4 years of age: consult a physician Adults and children over 2 years of age: apply generously rubbing into affected area as neededchildren 2 years of age: consult a physcian

    Which are Arnica Treatment Pack UNII Codes?

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

    Which are Arnica Treatment Pack 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.

    [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".