NDC 51393-5622 Eczema Control

Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, And Thuja Occidentalis Root

NDC Product Code 51393-5622

NDC Code: 51393-5622

Proprietary Name: Eczema Control What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, And Thuja Occidentalis Root 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.

NDC Code Structure

  • 51393 - Forces Of Nature
    • 51393-5622 - Eczema Control

NDC 51393-5622-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC 51393-5622-2

Package Description: 33 mL in 1 BOTTLE, DISPENSING

NDC 51393-5622-5

Package Description: 5 mL in 1 BOTTLE, DISPENSING

NDC Product Information

Eczema Control with NDC 51393-5622 is a 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.

Labeler Name: Forces Of Nature

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

Product Type: Human Otc Drug 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.

Eczema Control Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CENTELLA ASIATICA 12 [hp_C]/100mL
  • IRIS VERSICOLOR ROOT 12 [hp_C]/100mL
  • ARCTIUM LAPPA ROOT 12 [hp_C]/100mL
  • SODIUM CHLORIDE 12 [hp_X]/100mL
  • SILICON DIOXIDE 6 [hp_X]/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Forces Of Nature
Labeler Code: 51393
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 12-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Eczema Control Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index



Manufactured & Distributed byFORCES OF NATURE®21787 8th St East #3A Sonoma, CA 95476 USA

Otc - Purpose

Hydrocotyle AsiaticaCertified Organic 12C - Heals thickened and itchy skinSilicea 6X - Reduces inflammationNatrum Muriaticum 12X - Remedy for EczemaIris Versicolor 12C - Relieves itchy skin associated with EczemaLappa Articum 12C - Remedy for EczemaRuta Graveolens 12C - Relieves itchy skinTaraxacum Officinale 6C - Remedy for skin eruptionsThuja Occidentalis 8X - Relieves skin eruptions with itching

Also Contains

Sesame Oil, Lavandin Oil, Palmarosa Oil, Pine Oil, Rosemary Oil, Niaouli Oil, German Chamomile Oil


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


Apply to affected area by gently rubbing into the skin 3 or 4 times daily. For children under 2 years of age, consult a doctor before use.


Some individuals may be sensitive to essential oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin.For external use only. If accidental ingestion of more than several drops, and adverse reaction occurs, get medical help or contact a Poison Control Center. Do not apply to the eyes. If you are pregnant or breast -feeding, ask a health professional before use. Not for use on children under the age of 3.

Otc - Keep Out Of Reach Of Children

Keep all medicines out of the reach of children.

Otc - Stop Use

Stop use and consult a doctor if condition worsens, or consult a doctor if symptoms show no improvement after 7 days.

* Please review the disclaimer below.

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