NDC 43742-0957 Enviroclenz

Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Germanium Sesquioxide, Benzinum, Chlorinum, Acetone, Ammonium Muriaticum, Propylene Glycol, Sodium Benzene Sulfonate, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Belladonna, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum

NDC Product Code 43742-0957

NDC Code: 43742-0957

Proprietary Name: Enviroclenz 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, Carduus Marianus, Chelidonium Majus, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Stillingia Sylvatica, Taraxacum Officinale, Trifolium Pratense, Germanium Sesquioxide, Benzinum, Chlorinum, Acetone, Ammonium Muriaticum, Propylene Glycol, Sodium Benzene Sulfonate, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Methanol, Belladonna, Iridium Metallicum, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum 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

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0957 - Enviroclenz

NDC 43742-0957-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Enviroclenz with NDC 43742-0957 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Enviroclenz is berberis vulgaris, carduus marianus, chelidonium majus, glycyrrhiza glabra, lappa major, phytolacca decandra, rhamnus frangula, stillingia sylvatica, taraxacum officinale, trifolium pratense, germanium sesquioxide, benzinum, chlorinum, acetone, ammonium muriaticum, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, sodium tripolyphosphate, terebinthina, methanol, belladonna, iridium metallicum, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

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.

Enviroclenz 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
  • MILK THISTLE 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • FRANGULA ALNUS BARK 3 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
  • TARAXACUM OFFICINALE FLOWERING TOP 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE LEAF 3 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
  • BENZENE 9 [hp_X]/mL
  • CHLORINE 9 [hp_X]/mL
  • ACETONE 9 [hp_X]/mL
  • AMMONIUM CHLORIDE 9 [hp_X]/mL
  • PROPYLENE GLYCOL 9 [hp_X]/mL
  • SODIUM BENZENESULFONATE 9 [hp_X]/mL
  • SODIUM LAURYL SULFATE 9 [hp_X]/mL
  • SODIUM TRIPOLYPHOSPHATE 9 [hp_X]/mL
  • TURPENTINE OIL 9 [hp_X]/mL
  • METHYL ALCOHOL 9 [hp_X]/mL
  • ATROPA BELLADONNA 12 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [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.

Product Labeler Information

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

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 01-06-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-28-2022 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Enviroclenz Product Label Images

Enviroclenz 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, Carduus Marianus 3X, Chelidonium Majus 3X, Glycyrrhiza Glabra 3X, Lappa Major 3X, Phytolacca Decandra 3X, Rhamnus Frangula 3X, Stillingia Sylvatica 3X, Taraxacum Officinale 3X, Trifolium Pratense 3X, Germanium Sesquioxide 8X, Benzinum 9X, 12X, 15X, 30X, Chlorinum 9X, 12X, 15X, 30X, Acetone 9X, 12X, 15X, 30X, Ammonium Muriaticum 9X, 12X, 15X, 30X, Propylene Glycol 9X, 12X, 15X, 30X, Sodium Benzene Sulfonate 9X, 12X, 15X, 30X, Sodium Lauryl Sulfate 9X, 12X, 15X, 30X, Sodium Tripolyphosphate 9X, 12X, 15X, 30X, Terebinthina 9X, 12X, 15X, 30X, Methanol 9X, 12X, 15X, 30X, Belladonna 12X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Nitricum Acidum 12X, Nux Vomica 12X, Phosphoricum Acidum 12X.

Homeopathic Indications:

For temporary relief of symptoms related to toxicity caused by environmental substances including neck pain, hives, constipation, cough, and headache.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to toxicity caused by environmental substances including neck pain, hives, constipation, cough, and headache.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

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

Directions:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070      www.desbio.com

Package Label Display:

DESBIONDC 43742-0957-1HOMEOPATHICENVIROCLENZ1 FL OZ (30 ml)

* Please review the disclaimer below.

Previous Code
43742-0956
Next Code
43742-0958