Athletes Foot/jock Itch Control

Centella Asiatica, Silicon Dioxide, And Thuja Occidentalis Root

Forces Of Nature
Human Otc Drug
NDC 51393-7611

Athletes Foot/jock Itch Control also known as Centella Asiatica, Silicon Dioxide, And Thuja Occidentalis Root is a human otc drug labeled by 'Forces Of Nature'. National Drug Code (NDC) number for Athletes Foot/jock Itch Control is 51393-7611. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Athletes Foot/jock Itch Control drug includes Centella Asiatica Whole - 30 [hp_C]/1000mL Silicon Dioxide - 8 [hp_X]/1000mL Thuja Occidentalis Root - 30 [hp_C]/1000mL . The currest status of Athletes Foot/jock Itch Control drug is Active.

Drug Information:

Drug NDC:	51393-7611
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:	Athletes Foot/jock Itch Control
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	Athletes Foot/jock Itch
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	Control
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
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:	Centella Asiatica, Silicon Dioxide, And Thuja Occidentalis Root
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:	CENTELLA ASIATICA WHOLE - 30 [hp_C]/1000mL SILICON DIOXIDE - 8 [hp_X]/1000mL THUJA OCCIDENTALIS ROOT - 30 [hp_C]/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:	05 May, 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.
UNII:	7M867G6T1U ETJ7Z6XBU4 12958C0BR3
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.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
51393-7611-1	11 mL in 1 BOTTLE, DISPENSING (51393-7611-1)	01 Dec, 2011	N/A	No
51393-7611-2	33 mL in 1 BOTTLE, DISPENSING (51393-7611-2)	01 Dec, 2011	N/A	No
51393-7611-4	4 mL in 1 BOTTLE, DISPENSING (51393-7611-4)	15 Feb, 2017	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

Athletes Foot/jock Itch Control

Centella Asiatica, Silicon Dioxide, And Thuja Occidentalis Root

Solution/ Drops
Forces of Nature
NDC: 51393-7611

Purpose:

Active ingredients hydrocotyle asiatica usda certified organic 30c - remedy for itchy skin silicea 8x - anti-fungal remedy thuja occidentalis 30c - remedy for fungal related ailments

Product Elements:

Athletes foot/jock itch control centella asiatica, silicon dioxide, and thuja occidentalis root centella asiatica whole centella asiatica whole silicon dioxide silicon dioxide thuja occidentalis root thuja occidentalis root tea tree oil geranium oil, algerian type clove oil sesame oil

Indications and Usage:

Indications for the treatment of athlete's foot (tinea pedis) and jock itch (tinea cruris). relieves burning feet associated with athlete's foot and relieves the itching, burning, and irritation associated with jock itch.

Warnings:

Warnings 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 2 without physician direction. keep all medicines out of the reach of children. stop use and consult a doctor if condition worsens, or consult a doctor if symptoms show no improvement after 7 days.

Dosage and Administration:

Directions shake well before use. clean the affected area and dry thoroughly. apply a thin layer of product over the affected area 3 times daily. supervise children in the use of this product. for athlete's foot: pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. use daily for 4 weeks. for jock itch, use daily for 2 weeks. not to be used for diaper rash. if condition persists longer, consult a doctor. for children under 2 years of age, consult a doctor before use.

Stop Use:

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

Package Label Principal Display Panel:

Principal display panel - 4 ml bottle carton homeopathic ndc #51393-7611-4 forces of nature Â® certified organic medicine â athlete's foot rollerball applicator anti - fungal medicine quickly relieves itching & burning deep penetrating anti-fungal action soothes and promotes healthy skin fights both athletes foot & jock itch rare essential oils by elite growers from across the planet hydrocotyle asiatica usda organic .14 oz / 4 ml rollerball principal display panel - 4 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.