NDC 55138-007 Livergen

Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale

NDC Product Code 55138-007

NDC Code: 55138-007

Proprietary Name: Livergen 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: Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale 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

  • 55138 - Integra Health International, S.a. De C.v.
    • 55138-007 - Livergen

NDC 55138-007-02

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Livergen with NDC 55138-007 is a a human over the counter drug product labeled by Integra Health International, S.a. De C.v.. The generic name of Livergen is arnica montana, byronia alba root, silybum marianum seed, chelidonium majus, herring sperm dna, pork liver, cervus elaphus horn oil, sus scrofa pancreas, and taraxacum officinale. The product's dosage form is spray and is administered via oral form.

Labeler Name: Integra Health International, S.a. De C.v.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Livergen Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARNICA MONTANA 1.5 [hp_C]/30mL
  • BRYONIA ALBA ROOT 200 [hp_C]/30mL
  • CHELIDONIUM MAJUS 200 [hp_C]/30mL
  • HERRING SPERM DNA 3 [hp_C]/30mL
  • PORK LIVER 3 [hp_C]/30mL

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Integra Health International, S.a. De C.v.
Labeler Code: 55138
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 11-13-2013 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: 12-31-2017 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: E 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.

Livergen Product Label Images

Livergen 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 - Active Ingredient

Active Ingredients: Equal volumes of each ingredient: Arnica Montana 3X HPUS, Bryonia 200C HPUS, Carduus Marianus 1X HPUS, Chelidonium Majus 200C HPUS, DNA 6X HPUS, Hepar Suis 6X HPUS, Oleum Animale 8X HPUS, Pancreas Suis 8X HPUS, Taraxacum Officinale 2X HPUS.

Otc - Purpose

NDC #: 2728100296LIVERGENEnergy Medicine with DNAHomeopathic Fast-Acting Oral Spray1.0 Fl Oz (30 ml)Alcohol 9% v/v

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Indications & Usage

Indications: Helps detoxify the liver and temporarily relieves symptoms associated with an overworked or toxic liver, including: fatigue; poor sugar metabolism; poor liver function; ill effects of excessive alcohol consumption.

Dosage & Administration

Directions: Adults only: Spray twice under the tongue, three times a day. This bottle contains about a 1 month supply.


Warnings: Keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if symptoms persist more than 3 days, worsen, or if new symptoms occur.

Other Safety Information

Tamper Evident Seal: Do not use if seal around neck of bottle is broken or missing. The letters HPUS indicate that ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.

Inactive Ingredient

Inactive Ingredients: Alcohol 8% v/v, Glycerin 10% v/v, Purified Water.

* Please review the disclaimer below.

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