NDC 55758-318 Desintox

Antimonium Crudum,argentum Nitricum,cholesterinum, Robinia Pseudo-acacia,carbo Vegetabilis,cinchona,aesculus Hippocastanum,arnica Montana,berberis Vulgaris,ceanothus Americanus, Cynara Scolymus,equisetum Arvense,erigeron Canadensis,fucus Vesiculosus,ginkgo Biloba,hamamelis Virginiana,helonias Dioica,hydrastis Canadensis,hydrastis Canadensis,lappa Major,lespedeza Capitata,raphanus Sativus,taraxacum Officinale,viburnum Prunifolium,vitis Vinifera,ranunculus Bulbosus

NDC Product Code 55758-318

NDC Code: 55758-318

Proprietary Name: Desintox 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: Antimonium Crudum,argentum Nitricum,cholesterinum, Robinia Pseudo-acacia,carbo Vegetabilis,cinchona,aesculus Hippocastanum,arnica Montana,berberis Vulgaris,ceanothus Americanus, Cynara Scolymus,equisetum Arvense,erigeron Canadensis,fucus Vesiculosus,ginkgo Biloba,hamamelis Virginiana,helonias Dioica,hydrastis Canadensis,hydrastis Canadensis,lappa Major,lespedeza Capitata,raphanus Sativus,taraxacum Officinale,viburnum Prunifolium,vitis Vinifera,ranunculus Bulbosus 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

  • 55758 - Pharmadel Llc
    • 55758-318 - Desintox

NDC 55758-318-02

Package Description: 1 BOTTLE in 1 BOX > 60 mL in 1 BOTTLE

NDC Product Information

Desintox with NDC 55758-318 is a a human over the counter drug product labeled by Pharmadel Llc. The generic name of Desintox is antimonium crudum,argentum nitricum,cholesterinum, robinia pseudo-acacia,carbo vegetabilis,cinchona,aesculus hippocastanum,arnica montana,berberis vulgaris,ceanothus americanus, cynara scolymus,equisetum arvense,erigeron canadensis,fucus vesiculosus,ginkgo biloba,hamamelis virginiana,helonias dioica,hydrastis canadensis,hydrastis canadensis,lappa major,lespedeza capitata,raphanus sativus,taraxacum officinale,viburnum prunifolium,vitis vinifera,ranunculus bulbosus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Pharmadel Llc

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Desintox 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.

  • VITIS VINIFERA WHOLE 6 [hp_X]/60mL
  • CINCHONA BARK 8 [hp_X]/60mL
  • GOLDENSEAL 6 [hp_X]/60mL
  • RADISH 6 [hp_X]/60mL
  • HORSE CHESTNUT 6 [hp_X]/60mL
  • ANTIMONY TRISULFIDE 10 [hp_X]/60mL
  • ROBINIA PSEUDOACACIA BARK 10 [hp_X]/60mL
  • ACTIVATED CHARCOAL 9 [hp_X]/60mL
  • TARAXACUM OFFICINALE 6 [hp_X]/60mL
  • RANUNCULUS BULBOSUS 4 [hp_X]/60mL
  • CYNARA SCOLYMUS LEAF 6 [hp_X]/60mL
  • CHAMAELIRIUM LUTEUM ROOT 6 [hp_X]/60mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/60mL
  • LESPEDEZA CAPITATA FLOWERING TOP 6 [hp_X]/60mL
  • VIBURNUM PRUNIFOLIUM BARK 6 [hp_X]/60mL
  • SILVER NITRATE 10 [hp_X]/60mL
  • ARNICA MONTANA 6 [hp_X]/60mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/60mL
  • ERIGERON CANADENSIS 6 [hp_X]/60mL
  • CEANOTHUS AMERICANUS LEAF 6 [hp_X]/60mL
  • EQUISETUM ARVENSE TOP 6 [hp_X]/60mL
  • FUCUS VESICULOSUS 6 [hp_X]/60mL
  • GINKGO 10 [hp_X]/60mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 6 [hp_X]/60mL

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.

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

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: Pharmadel Llc
Labeler Code: 55758
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: 01-01-2019 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: 12-31-2020 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: N 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.

Desintox Product Label Images

Desintox 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

Active ingredients** HPUS (per 20 drops)Purpose*Antimonium crudum 10x, Argentum nitricum 10x,Cholesterinum 10x,Robinia pseudo-acacia 10x, Carbo vegetabilis 9x, Cinchona 8x,Aesculus hippocastanum 6x, Arnica montana 6x, Berberis vulgaris 6x,Ceanothus americanus 6x,Cynara scolymus 6x, Equisetum arvense 6x,Erigeron canadensis 6x, Fucus vesiculosus 6x, Ginkgo biloba 10x,Hamamelis virginiana 6x, Helonias dioica 6x,Hydrastis canadensis 6x,Lappa major6x,Lespedeza capitata 6x, Raphanus sativus 6x, Taraxacum officinale 6x,Viburnum prunifolium 6x, Vitis vinifera 6x, Ranunculus bulbosus 4xHelpsdetoxification bystimulating excretory organsThe letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopeia of the United States.

Uses*

Relieves symptoms caused by unbalanced diet, exposure to environmental toxins, use of medications including vaccinations, smoking and alcohol consumption.

Stop Use And Ask A Doctor If

  • Symptoms persist, reoccur or worsens an allergic reaction occurs, seek medical help right away

If Pregnant Or Breastfeeding,

Ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • Shake well before each useadults and children over 12 years of age: place 20 drops in a small glass of water two (2) times a day, 15 minutes before a mealallow medicine to remain in the mouth for 15 seconds before swallowing

Other Information

  • Store at room temperature 59°­86°F (15°-30°C)Tamper Evident: Do not use if seal is torn, broken, or missing.

Inactive Ingredients

Purified water, alcohol 20%

* Please review the disclaimer below.

Previous Code
55758-317
Next Code
55777-0100