NDC 43742-1560 Enviro I

Potassium Gluconate, Glandula Suprarenalis Suis, Hepar Suis, Coffea Tosta, Thea Sinensis, Carbo Vegetabilis, Ferrum Iodatum, Ferrum Metallicum, Gelsemium Sempervirens, Iodium, Iridium Metallicum, Lycopodium Clavatum, Pulsatilla (vulgaris), Selenium Metallicum, Zincum Metallicum, Peanut, Black Walnut, English Walnut, Almond, Cashew, Coconut, Pecan, Brazil Nut, Tomato, Potato, Black Pepper, Eggplant, Rape Seed Oil, Sesame, Seed, Cheese (stilton), Lac Vaccinum, Beef, Lamb, Pork, Chicken, Egg (whole), Phaseolus Liquid Oral

NDC Product Code 43742-1560

NDC CODE: 43742-1560

Proprietary Name: Enviro I 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: Potassium Gluconate, Glandula Suprarenalis Suis, Hepar Suis, Coffea Tosta, Thea Sinensis, Carbo Vegetabilis, Ferrum Iodatum, Ferrum Metallicum, Gelsemium Sempervirens, Iodium, Iridium Metallicum, Lycopodium Clavatum, Pulsatilla (vulgaris), Selenium Metallicum, Zincum Metallicum, Peanut, Black Walnut, English Walnut, Almond, Cashew, Coconut, Pecan, Brazil Nut, Tomato, Potato, Black Pepper, Eggplant, Rape Seed Oil, Sesame, Seed, Cheese (stilton), Lac Vaccinum, Beef, Lamb, Pork, Chicken, Egg (whole), Phaseolus 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 43742-1560-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Enviro I with NDC 43742-1560 is a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Enviro I is potassium gluconate, glandula suprarenalis suis, hepar suis, coffea tosta, thea sinensis, carbo vegetabilis, ferrum iodatum, ferrum metallicum, gelsemium sempervirens, iodium, iridium metallicum, lycopodium clavatum, pulsatilla (vulgaris), selenium metallicum, zincum metallicum, peanut, black walnut, english walnut, almond, cashew, coconut, pecan, brazil nut, tomato, potato, black pepper, eggplant, rape seed oil, sesame, seed, cheese (stilton), lac vaccinum, beef, lamb, pork, chicken, egg (whole), phaseolus. The product's dosage form is liquid and is administered via oral form.

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.

Enviro I 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.


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.

Pharmacologic Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.


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: 09-05-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-12-2024 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Enviro I Product Label Images

Enviro I 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:

Potassium Gluconate 6X, Glandula Suprarenalis Suis 8X, Hepar Suis 8X, Coffea Tosta 10X, 12X, 15X, 30X, Thea Sinensis 10X, 12X, 15X, 30X, Carbo Vegetabilis 12X, Ferrum Iodatum 12X, Ferrum Metallicum 12X, Gelsemium Sempervirens 12X, Iodium 12X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Pulsatilla (Vulgaris) 12X, Selenium Metallicum 12X, Zincum Metallicum 12X, Peanut 12X, 30X, Black Walnut 12X, 30X, English Walnut 12X, 30X, Almond 12X, 30X, Cashew 12X, 30X, Coconut 12X, 30X, Pecan 12X, 30X, Brazil Nut 12X, 30X, Potato 12X, 30X, Black Pepper 12X, 30X, Eggplant 12X, 30X, Rape Seed Oil 12X, 30X, Flax Seed 12X, 30X, Sesame Seed 12X, 30X, Cheese (Stilton) 12X, 30X,Lac Vaccinum 12X, 30X, Beef 12X, 30X, Lamb 12X, 30X, Chicken 12X, 30X, Egg (Whole) 12X, 30X, Phaseolus 12X, 30X, Allium Cepa 12X, 30X, Apple 12X, 30X,Wheat 12X, 30X, Banana 12X, 30X, Strawberry 12X, 30X, Orange 12X, 30X, Cod (Gadus Morrhua)12X, 30X, Tuna (Thunnus Thynnus) 12X, 30X, Salmon (Salmo Salar) 12X, 30X, Crab Cancer Pagurus) 12X, 30X, Oyster (Crassostrea Gigas) 12X, 30X, Shrimp (Crangon Crangon) 12X, 30X, Cortisone Aceticum 30X, Histaminum Hydrochloricum 30X, Hyaluronidase 30X, Interferon (Suis) 30X, Serotonin (Hydrochloride) 30X, Cacao 10C, 12C, 15C, 30C.

Homeopathic Indications:

For temporary relief of symptoms related to food allergies including swelling of the lips, stomach cramps, vomiting, occasional diarrhea, and skin rashes .****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 food allergies including swelling of the lips, stomach cramps, vomiting, occasional diarrhea, and skin rashes .****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 43742-1560-1HOMEOPATHICENVIRO I1 FL OZ (30 ml)

* Please review the disclaimer below.