NDC 68703-105 Varicogo

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  2. Native Remedies, Llc
  3. NDC: 68703-105 Varicogo

NDC Product Code 68703-105

NDC CODE: 68703-105

Proprietary Name: Varicogo 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: 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

  • 68703 - Native Remedies, Llc

NDC 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.

NDC Product Information

Varicogo with NDC 68703-105 is a product labeled by Native Remedies, Llc. The generic name of Varicogo is . The product's dosage form is and is administered via form.

Labeler Name: Native Remedies, Llc

Dosage Form: -

Product Type: 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.

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.
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Native Remedies, Llc
Labeler Code: 68703
Start Marketing Date: 06-26-2013 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: 12-31-2018 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: I 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.

Varicogo Product Label Images

Varicogo 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

Otc - Purpose

Relieves discomfort associated with varicose veins

Otc - Active Ingredient

Drug FactsActive 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.comDistributed  byNative Remedies, LLC6531 Park of Commerce Blvd.Suite 160Boca Raton, FL 33487Phone:+1.877.289.1235International:1.561.999.8857No gluten, artificial flavors, or colorants added

Storage And Handling

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

* Please review the disclaimer below.