NDC 68703-105 Varicogo

Product Information

What is NDC 68703-105?

The NDC code 68703-105 is assigned by the FDA to the product Varicogo which is product labeled by Native Remedies, Llc. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 68703-105-59 59 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code68703-105
Proprietary Name 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.		Varicogo
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Native Remedies, Llc
Labeler Code68703
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		06-26-2013
Listing Expiration Date 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.		12-31-2018
Exclude Flag 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". 		I
NDC Code Structure

What are the uses for Varicogo?


Product Packages

NDC Code 68703-105-59

Package Description: 59 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Varicogo Active Ingredients UNII Codes

Varicogo 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.

* Please review the disclaimer below.

Varicogo Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Otc - Purpose



Relieves discomfort associated with varicose veins


Otc - Active Ingredient



Drug Facts
Active Ingredients: Equal volumes of each ingredient in 10X, 30X, LM10 potencies: Aesculus hippocastanum, Arnica montana, Calcarea fluorica, Carduus marianus, Carbo vegetabilis, Collinsonia canadensis, Echinacea purpurea, Hamamelis virginiana, Lachesis mutus, Pulsatilla, Secale cornutum


Indications & Usage



Uses: For temporary relief of discomforts associated with varicose veins: cramping in lower extremities, aching or soreness in limbs, enlarged veins, congested veins, and tiredness in legs


Warnings



Warnings: Stop use and ask a doctor if symptoms persist or worsen


Otc - Pregnancy Or Breast Feeding



If pregnant or breastfeeding,  ask a health professional before use


Otc - Keep Out Of Reach Of Children



Keep this and all medication out of reach of children


Overdosage



In case of overdose, get medical help or contact a Poison Control Center right away


Dosage & Administration



Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed. Adults: 3 pump sprays. Children 2-12: 2 pump sprays


Inactive Ingredient



Inactive Ingredients: Citric acid, potassium sorbate, pure water


Information For Patients



The lleters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed  by
Native Remedies, LLC
6531 Park of Commerce Blvd.
Suite 160
Boca Raton, FL 33487
Phone:+1.877.289.1235
International:1.561.999.8857

No gluten, artificial flavors, or colorants added


Storage And Handling



Tamper resistant for your protection. Use only if safety seal is intact


Package Label.Principal Display Panel



Bottle Label - VVG001

Bottle Label - VVG001


* Please review the disclaimer below.