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 (pratensis), Selenium Metallicum, Zincum Metallicum, Peanut, Black Walnut, English Walnut, Amygdala Amara, Cashew, Coconut, Pecan, Brazil Nut, Tomato, Solanum Tuberosum, Piper Nigrum, Eggplant, Rape Seed Oil, Linum Usitatissimum, Sesame, Seed, Cheese (stilton), Lac Vaccinum, Beef,

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1950

Enviro I also known as 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 (pratensis), Selenium Metallicum, Zincum Metallicum, Peanut, Black Walnut, English Walnut, Amygdala Amara, Cashew, Coconut, Pecan, Brazil Nut, Tomato, Solanum Tuberosum, Piper Nigrum, Eggplant, Rape Seed Oil, Linum Usitatissimum, Sesame, Seed, Cheese (stilton), Lac Vaccinum, Beef, is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Enviro I is 43742-1950. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Enviro I drug includes Activated Charcoal - 12 [hp_X]/mL Anemone Pratensis - 12 [hp_X]/mL Apple - 12 [hp_X]/mL Atlantic Cod - 12 [hp_X]/mL Atlantic Salmon - 12 [hp_X]/mL Banana - 12 [hp_X]/mL Beef - 12 [hp_X]/mL Bitter Almond - 12 [hp_X]/mL Black Walnut - 12 [hp_X]/mL Brazil Nut - 12 [hp_X]/mL and more. The currest status of Enviro I drug is Active.

Drug Information:

Drug NDC:	43742-1950
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Enviro I
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
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 (pratensis), Selenium Metallicum, Zincum Metallicum, Peanut, Black Walnut, English Walnut, Amygdala Amara, Cashew, Coconut, Pecan, Brazil Nut, Tomato, Solanum Tuberosum, Piper Nigrum, Eggplant, Rape Seed Oil, Linum Usitatissimum, Sesame, Seed, Cheese (stilton), Lac Vaccinum, Beef,
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ACTIVATED CHARCOAL - 12 [hp_X]/mL ANEMONE PRATENSIS - 12 [hp_X]/mL APPLE - 12 [hp_X]/mL ATLANTIC COD - 12 [hp_X]/mL ATLANTIC SALMON - 12 [hp_X]/mL BANANA - 12 [hp_X]/mL BEEF - 12 [hp_X]/mL BITTER ALMOND - 12 [hp_X]/mL BLACK WALNUT - 12 [hp_X]/mL BRAZIL NUT - 12 [hp_X]/mL Load more... CANOLA OIL - 12 [hp_X]/mL CASEIN, LACTOCOCCUS LACTIS CULTURED, PENICILLIUM ROQUEFORTI CULTURED, AGED - 12 [hp_X]/mL CASHEW - 12 [hp_X]/mL CHICKEN - 12 [hp_X]/mL COCOA - 10 [hp_C]/mL COCONUT - 12 [hp_X]/mL COFFEA ARABICA SEED, ROASTED - 10 [hp_X]/mL COMMON SHRIMP - 12 [hp_X]/mL CORTISONE ACETATE - 30 [hp_X]/mL COW MILK - 12 [hp_X]/mL EDIBLE ROCK CRAB - 12 [hp_X]/mL EGG - 12 [hp_X]/mL EGGPLANT - 12 [hp_X]/mL ENGLISH WALNUT - 12 [hp_X]/mL FERROUS IODIDE - 12 [hp_X]/mL FLAX SEED - 12 [hp_X]/mL FRAGARIA VESCA FRUIT - 12 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT - 12 [hp_X]/mL GREEN PEPPERCORN - 12 [hp_X]/mL GREEN TEA LEAF - 10 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE - 30 [hp_X]/mL HYALURONIDASE - 30 [hp_X]/mL INTERFERON .GAMMA. PORCINE RECOMBINANT - 30 [hp_X]/mL IODINE - 12 [hp_X]/mL IRIDIUM - 12 [hp_X]/mL IRON - 12 [hp_X]/mL KIDNEY BEAN - 12 [hp_X]/mL LAMB - 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL NORTHERN BLUEFIN TUNA - 12 [hp_X]/mL ONION - 12 [hp_X]/mL ORANGE - 12 [hp_X]/mL PACIFIC OYSTER - 12 [hp_X]/mL PEANUT - 12 [hp_X]/mL PECAN - 12 [hp_X]/mL PORK - 12 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL POTASSIUM GLUCONATE - 6 [hp_X]/mL SELENIUM - 12 [hp_X]/mL SEROTONIN HYDROCHLORIDE - 30 [hp_X]/mL SESAME SEED - 12 [hp_X]/mL SOLANUM TUBEROSUM WHOLE - 12 [hp_X]/mL SUS SCROFA ADRENAL GLAND - 8 [hp_X]/mL TOMATO - 12 [hp_X]/mL WHEAT - 12 [hp_X]/mL ZINC - 12 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	26 Feb, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	07 May, 2026
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.
Listing Expiration Date:	31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185371 N0000175629 M0000728 M0006342 N0000185015 N0000184306 N0000185014 N0000185017 N0000185019 N0000185018 M0016962 M0013890 M0023708 N0000185375 M0022575 N0000185001 M0516536 N0000175531 M0009499 N0000185016
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	2P3VWU3H10 8E272251DI B423VGH5S9 RPX7J99EXW 7062I37LB3 4AJZ4765R9 4PIB2155QP O65SFW8R9A 02WM57RXZJ XKR79OET1K Load more... 331KBJ17RK IYI0G2057S 3H5U5CX7KO 0X8Q245Y7B D9108TZ9KG 3RT3536DHY 9H58JRT35E 1U601HV1HW 883WKN7W8X 917J3173FT RLE491K17W 291P45F896 W5K7RAS4VK 1V3SHR7QB7 F5452U54PN 4110YT348C CG6IX3GCMU 639KR60Q1Q 6G53L8ESRK W2ZU1RY8B0 3POA0Q644U 8KOG53Z5EM 69404B0LO7 9679TC07X4 44448S9773 E1UOL152H7 M98C8416QO FOF26T73HA C88X29Y479 816CLQ4017 492225Q21H 5EVU04N5QU FX2S0D3781 QE1QX6B99R F14P91GB5F O138UB266J 6EC706HI7F 12H3K5QKN9 H6241UJ22B GKN429M9VS 7Y1255HVXR 2A8I57T4MX 398IYQ16YV Z4KHF2C175 4J2I0SN84Y J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Endoglycosidase [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Plant Proteins [CS] Milk Proteins [CS] Egg Proteins, Dietary [CS] Vegetable Proteins [CS] Seed Storage Proteins [CS] Glycoside Hydrolases [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Cell-mediated Immunity [PE] Corticosteroid Hormone Receptor Agonists [MoA] Corticosteroid [EPC] Dietary Proteins [CS] Egg Proteins Dietary [CS] Endoglycosidase [EPC] Fish Proteins Dietary [EXT] Fruit Proteins [EXT] Glycoside Hydrolases [CS] Grain Proteins [EXT] Increased Histamine Release [PE] Increased IgG Production [PE] Increased Large Intestinal Motility [PE] Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] Meat Proteins [EXT] Milk Proteins [CS] Non-Standardized Food Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1950-1	30 mL in 1 BOTTLE, DROPPER (43742-1950-1)	26 Feb, 2021	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Enviro I

Potassium Gluconate & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1950

Purpose:

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 homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

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 (pratensis), selenium metallicum, zincum metallicum, peanut, black walnut, english walnut, amygdala amara, cashew, coconut, pecan, brazil nut, tomato, solanum tuberosum, piper nigrum, eggplant, rape seed oil, linum usitatissimum, sesame, seed, cheese (stilton), lac vaccinum, beef, potassium gluconate potassium cation sus scrofa adrenal gland sus scrofa adrenal gland pork liver pork liver coffea arabica seed, roasted coffea arabica seed, roasted green tea leaf green tea leaf activated charcoal activated charcoal ferrous iodide ferrous iodide iron iron gelsemium sempervirens root gelsemium sempervirens root iodine iodine iridium iridium lycopodium clavatum spore lycopodium clavatum spore anemone pratensis anemone pratensis selenium selenium zinc zinc peanut peanut black walnut black walnut english walnut english walnut bitter almond bitter almond cashew cashew coconut coconut pecan pecan brazil nut brazil nut tomato tomato solanum tuberosum whole solanum tuberosum whole green peppercorn green peppercorn eggplant eggplant canola oil canola oil flax seed flax seed sesame seed sesame seed casein, lactococcus lactis cultured, penicillium roqueforti cultured, aged casein, lactococcus lactis cultured, penicillium roqueforti cultured, aged cow milk cow milk beef beef lamb lamb pork pork chicken chicken egg egg kidney bean kidney bean onion onion apple apple wheat wheat banana banana fragaria vesca fruit alpine strawberry orange orange atlantic cod atlantic cod northern bluefin tuna northern bluefin tuna atlantic salmon atlantic salmon edible rock crab edible rock crab pacific oyster pacific oyster common shrimp common shrimp cortisone acetate cortisone histamine dihydrochloride histamine hyaluronidase hyaluronidase interferon .gamma. porcine recombinant interferon .gamma. porcine recombinant serotonin hydrochloride serotonin cocoa cocoa water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or 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.

Dosage and Administration:

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.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1950-1 homeopathic enviro i 1 fl oz (30 ml) enviro i

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.