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NDC 60986-1032 Polygonum

Polygonum Aviculare,Acorus Calamus,Rhus Toxicodendron,Gnaphalium Polycephalum,Rhododendron - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60986-1032?
  4. Polygonum Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
60986-1032
Proprietary Name:
Polygonum
Non-Proprietary Name: [1]
Polygonum Aviculare, Acorus Calamus, Rhus Toxicodendron, Gnaphalium Polycephalum, Rhododendron Chrysanthum, Colocynthis, Colchicum Autumnale, Kali Iodatum, Ichthyolum, Symphytum Officinale
Substance Name: [2]
Acorus Calamus Whole; Citrullus Colocynthis Fruit Pulp; Colchicum Autumnale Bulb; Comfrey Root; Ichthammol; Polygonum Aviculare Top; Potassium Iodide; Pseudognaphalium Obtusifolium; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Marco Pharma International Llc.
    Labeler Code:
    60986
    Product Label ID:
    e1711c08-0dfc-6267-e053-2a95a90a1cd7
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    06-14-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 60986-1032-3

    Package Description: 50 mL in 1 BOTTLE, GLASS

    NDC Code 60986-1032-4

    Package Description: 100 mL in 1 BOTTLE, GLASS

    Product Details

    What is NDC 60986-1032?

    The NDC code 60986-1032 is assigned by the FDA to the product Polygonum which is a human over the counter drug product labeled by Marco Pharma International Llc.. The generic name of Polygonum is polygonum aviculare, acorus calamus, rhus toxicodendron, gnaphalium polycephalum, rhododendron chrysanthum, colocynthis, colchicum autumnale, kali iodatum, ichthyolum, symphytum officinale. The product's dosage form is liquid and is administered via oral form. The product is distributed in 2 packages with assigned NDC codes 60986-1032-3 50 ml in 1 bottle, glass , 60986-1032-4 100 ml in 1 bottle, glass . 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 Polygonum?

    Indications: For temporary relief of pain in joints and muscles.

    What are Polygonum 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 Polygonum UNII Codes?

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

    Which are Polygonum 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".