Ringworm Control

Thuja Occidentalis Leaf, Silicon Dioxide, And Sodium Chloride

Forces Of Nature
Human Otc Drug
NDC 51393-7599

Ringworm Control also known as Thuja Occidentalis Leaf, Silicon Dioxide, And Sodium Chloride is a human otc drug labeled by 'Forces Of Nature'. National Drug Code (NDC) number for Ringworm Control is 51393-7599. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Ringworm Control drug includes Silicon Dioxide - 10 [hp_X]/1000mL Sodium Chloride - 10 [hp_X]/1000mL Thuja Occidentalis Leaf - 10 [hp_X]/1000mL . The currest status of Ringworm Control drug is Active.

Drug Information:

Drug NDC:	51393-7599
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Ringworm Control
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Thuja Occidentalis Leaf, Silicon Dioxide, And Sodium Chloride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Forces Of Nature
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution/ Drops
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	SILICON DIOXIDE - 10 [hp_X]/1000mL SODIUM CHLORIDE - 10 [hp_X]/1000mL THUJA OCCIDENTALIS LEAF - 10 [hp_X]/1000mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	01 Dec, 2011
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	09 Jun, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Forces of Nature
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0830743009028
UPC stands for Universal Product Code.
UNII:	ETJ7Z6XBU4 451W47IQ8X 0T0DQN8786
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:	Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Osmotic Activity [MoA] Osmotic Laxative [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
51393-7599-1	11 mL in 1 BOTTLE, DISPENSING (51393-7599-1)	01 Dec, 2011	N/A	No
51393-7599-2	33 mL in 1 BOTTLE, DISPENSING (51393-7599-2)	01 Dec, 2011	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Ringworm Control

Thuja Occidentalis Leaf, Silicon Dioxide, And Sodium Chloride

Solution/ Drops
Forces of Nature
NDC: 51393-7599

Purpose:

Active ingredients purpose thuja occidentalis certified organic 10x remedy for ringworm silica 10x remedy for itchy skin natrum muriaticum 10x ringworm remedy

Product Elements:

Ringworm control thuja occidentalis leaf, silicon dioxide, and sodium chloride thuja occidentalis leaf thuja occidentalis leaf silicon dioxide silicon dioxide sodium chloride sodium cation sesame oil tea tree oil geranium oil, algerian type clove oil thyme oil

Indications and Usage:

Indications for the treatment of ringworm (tinea corporis).

Warnings:

Warnings for external use only. avoid contact with the eyes; in the event of contact, flush with water and seek advice from medical personnel. if irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor. some individuals may be sensitive to tea tree or other oils. if you are pregnant or breast-feeding, ask a health professional before use. not to be used with children under 2 years of age without physician direction. do not use for diaper rash. keep all medicines out of the reach of children.

Do Not Use:

When Using:

Avoid contact with the eyes; in the event of contact, flush with water and seek advice from medical personnel.

Some individuals may be sensitive to tea tree or other oils.

Dosage and Administration:

Directions clean the affected area and dry thoroughly. apply a thin layer of the product over affected area and rub gently into the skin 3 times daily or as directed by a doctor. supervise children in the use of this product. if condition persists longer than 4 weeks, consult a doctor.

Stop Use:

If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor.

Package Label Principal Display Panel:

Principal display panel - 11 ml bottle carton ndc#: 51393-7599-1 guaranteed forces of nature Â® ringworm control safe and effective ringworm treatment rejuvenates damaged skin provides fast acting results penetrates deep into the skin homeopathic medicine fda registered + usda organic homeopathic medicine â¢ certified organic 11 ml principal display panel - 11 ml bottle carton

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.