NDC 51393-5622 Eczema Control

Centella Asiatica,Iris Versicolor Root,Arctium Lappa Root,Sodium Chloride,Ruta Graveolens - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
51393-5622
Proprietary Name:
Eczema Control
Non-Proprietary Name: [1]
Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, And Thuja Occidentalis Root
Substance Name: [2]
Arctium Lappa Root; Centella Asiatica Whole; Iris Versicolor Root; Ruta Graveolens Flowering Top; Silicon Dioxide; Sodium Chloride; Taraxacum Officinale; Thuja Occidentalis Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • 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]
    Forces Of Nature
    Labeler Code:
    51393
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-01-2011
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Packages

    NDC Code 51393-5622-1

    Package Description: 11 mL in 1 BOTTLE, DISPENSING

    NDC Code 51393-5622-2

    Package Description: 33 mL in 1 BOTTLE, DISPENSING

    NDC Code 51393-5622-3

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    NDC Code 51393-5622-5

    Package Description: 5 mL in 1 BOTTLE, DISPENSING

    Product Details

    What is NDC 51393-5622?

    The NDC code 51393-5622 is assigned by the FDA to the product Eczema Control which is a human over the counter drug product labeled by Forces Of Nature. The generic name of Eczema Control is centella asiatica, iris versicolor root, arctium lappa root, sodium chloride, ruta graveolens flowering top, silicon dioxide, taraxacum officinale, and thuja occidentalis root. The product's dosage form is solution/ drops and is administered via topical form. The product is distributed in 4 packages with assigned NDC codes 51393-5622-1 11 ml in 1 bottle, dispensing , 51393-5622-2 33 ml in 1 bottle, dispensing , 51393-5622-3 30 ml in 1 bottle, dropper , 51393-5622-5 5 ml in 1 bottle, dispensing . 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 Eczema Control?

    For the temporary relief of itching associated with minor skin irritations and rashes which may be due to Eczema.

    What are Eczema Control 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 Eczema Control UNII Codes?

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

    Which are Eczema Control 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".