NDC 73518-0001 Chemtox

Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum, Camphora, Cysteinum, Nux Vomica, Sulphuricum Acidum, Acetaldehyde, Benzinum, Calcarea Carbonica, Carbolicum Acidum, Kreosotum, Lachesis Mutus, Naphthalinum, Plumbum Metallicum, Formalinum, Carboneum Chloratum, Chloroformum, Etherum, Paraffinum, Petroleum

NDC Product Code 73518-0001

NDC CODE: 73518-0001

Proprietary Name: Chemtox 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: Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum, Camphora, Cysteinum, Nux Vomica, Sulphuricum Acidum, Acetaldehyde, Benzinum, Calcarea Carbonica, Carbolicum Acidum, Kreosotum, Lachesis Mutus, Naphthalinum, Plumbum Metallicum, Formalinum, Carboneum Chloratum, Chloroformum, Etherum, Paraffinum, Petroleum 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

NDC 73518-0001-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Chemtox with NDC 73518-0001 is a a human over the counter drug product labeled by Energenx Llc. The generic name of Chemtox is berberis vulgaris, taraxacum officinale, ammonium carbonicum, camphora, cysteinum, nux vomica, sulphuricum acidum, acetaldehyde, benzinum, calcarea carbonica, carbolicum acidum, kreosotum, lachesis mutus, naphthalinum, plumbum metallicum, formalinum, carboneum chloratum, chloroformum, etherum, paraffinum, petroleum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energenx 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.

Chemtox 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.

  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • AMMONIUM CARBONATE 6 [hp_X]/mL
  • CAMPHOR (NATURAL) 6 [hp_X]/mL
  • CYSTEINE 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • SULFURIC ACID 6 [hp_X]/mL
  • ACETALDEHYDE 12 [hp_X]/mL
  • BENZENE 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • PHENOL 12 [hp_X]/mL
  • WOOD CREOSOTE 12 [hp_X]/mL
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • NAPHTHALENE 12 [hp_X]/mL
  • LEAD 12 [hp_X]/mL
  • FORMALDEHYDE SOLUTION 12 [hp_X]/mL
  • CARBON TETRACHLORIDE 16 [hp_X]/mL
  • CHLOROFORM 16 [hp_X]/mL
  • ETHER 16 [hp_X]/mL
  • PARAFFIN 16 [hp_X]/mL
  • KEROSENE 16 [hp_X]/mL

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.
  • 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: Energenx Llc
Labeler Code: 73518
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: 07-14-2020 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: 12-31-2021 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.

Chemtox Product Label Images

Chemtox 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

Active Ingredients:

Berberis Vulgaris 3X, Taraxacum Officinale 3X, Ammonium Carbonicum 6X, Camphora 6X, Cysteinum 6X, Nux Vomica 6X, Sulphuricum Acidum 6X, 12X, Acetaldehyde 12X, Benzinum 12X, Calcarea Carbonica 12X, Carbolicum Acidum 12X, Kreosotum 12X, Lachesis Mutus 12X, Naphthalinum 12X, Plumbum Metallicum 12X, Formalinum 12X, 30X, Carboneum Chloratum 16X, Chloroformum 16X, Etherum 16X, 20X, 30X, 60X, Paraffinum16X, 20X, 30X, 60X, Petroleum 16X, 20X, 30X, 60X.

Indications:

For symptom relief due to environmental toxin exposure.****These statements are based upon traditional homeopathic practices. They have not been reviewed by the Food and Drug Administration.

For symptom relief due to environmental toxin exposure.****These statements are based upon traditional homeopathic practices. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breast-feeding, ask a health care professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Store in a cool, dry place.Do not use if tamper-evident seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Take 10 drops 3x's per day under tongue until finished. Repeat every 3-4 months or as suggested by your healthcare provider. Consume 30 minutes from food, liquid, or toothpaste. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 20% Gluten-Free Organic Ethanol

Questions:

Distributed by Energenx, LLC225 Walnut StreetMontclair, NJ 07042www.energenx.org

Package Label Display:

ENERGENXCHEMTOXHOMEOPATHIC REMEDY2fl.oz/60 ml

* Please review the disclaimer below.