Varicose Veins Control

Horse Chestnut, Milk Thistle, And Hamamelis Virginiana Root Bark/stem Bark

Forces Of Nature
Human Otc Drug
NDC 51393-8111

Varicose Veins Control also known as Horse Chestnut, Milk Thistle, And Hamamelis Virginiana Root Bark/stem Bark is a human otc drug labeled by 'Forces Of Nature'. National Drug Code (NDC) number for Varicose Veins Control is 51393-8111. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in Varicose Veins Control drug includes Hamamelis Virginiana Root Bark/stem Bark - 30 [hp_C]/100mL Horse Chestnut - 30 [hp_C]/100mL Milk Thistle - 12 [hp_C]/100mL . The currest status of Varicose Veins Control drug is Active.

Drug Information:

Drug NDC:	51393-8111
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:	Varicose Veins Control
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	Varicose Veins
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:	Horse Chestnut, Milk Thistle, And Hamamelis Virginiana Root Bark/stem Bark
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:	HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 30 [hp_C]/100mL HORSE CHESTNUT - 30 [hp_C]/100mL MILK THISTLE - 12 [hp_C]/100mL
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:	24 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:	0830743011366
UPC stands for Universal Product Code.
UNII:	T7S323PKJS 3C18L6RJAZ U946SH95EE
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
51393-8111-1	11 mL in 1 BOTTLE, DISPENSING (51393-8111-1)	01 Dec, 2011	N/A	No
51393-8111-2	33 mL in 1 BOTTLE, DISPENSING (51393-8111-2)	01 Dec, 2011	N/A	No
51393-8111-3	30 mL in 1 BOTTLE, DISPENSING (51393-8111-3)	01 Aug, 2021	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

Varicose Veins Control

Horse Chestnut, Milk Thistle, And Hamamelis Virginiana Root Bark/stem Bark

Solution/ Drops
Forces of Nature
NDC: 51393-8111

Purpose:

Active ingredients purpose aesculus hippocastanum usda certified organic 30c remedy for varicose veins carduus marianus 12c treats varicose veins/vascular deficiency hamamelis virginiana 30c treats varicose veins/venous congestion

Product Elements:

Varicose veins control horse chestnut, milk thistle, and hamamelis virginiana root bark/stem bark horse chestnut horse chestnut milk thistle milk thistle hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark geranium oil, algerian type cupressus sempervirens leaf oil niaouli oil sesame oil

Indications and Usage:

Uses topical analgesic for the temporary relief of minor aches, pains, and blemishes associated with varicose veins.

Warnings:

Warnings for external use only. some individuals may be sensitive to essential oils. begin with a small drop to determine if product causes any irritation. discontinue use if any irritation occurs. stop use and consult a doctor if condition worsens. not for use on children under the age of 2 without physician direction. keep out of reach of children. if pregnant or breast-feeding, ask a health professional before use. if accidental ingestion and adverse reaction occurs, get medical help or contact a poison control center.

Dosage and Administration:

Directions shake well before use. apply to affected area by gently rubbing into the skin up to 3 or 4 times daily until symptoms have cleared.

Package Label Principal Display Panel:

Principal display panel - 11 ml bottle carton homeopathic ndc #51393-8111-1 forces of nature Â® certified organic medicineâ varicose vein control 11 ml topical varicose vein medicine treats spider / varicose veins helps shrink enlarged veins delivers rapid results highly concentrated carduus marianus usda organic .37 oz/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.