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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 Metal 6 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 10 [hp_X]/mL; 10 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL Liquid, 30 mL

by Deseret Biologicals, Inc. · 30 mL in 1 BOTTLE, DROPPER (43742-1950-1)
NDC 43742-1950-01
🏷️ FDA NDC (as labeled) 43742-1950-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 43742-1950-1
Product NDC 43742-1950
11-digit billing NDC 43742195001
UNII 12H3K5QKN9, 398IYQ16YV, 6EC706HI7F, 9H58JRT35E, W2ZU1RY8B0, 2P3VWU3H10 +12 more
SPL Set ID 1de4f602-6e3c-4142-b60a-90585ac33884
Established class (EPC) Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Endoglycosidase
Physiologic effect Increased Histamine Release; Cell-mediated Immunity; Increased IgG Production
Chemical class Allergens; Dietary Proteins; Vegetable Proteins; Plant Proteins; Seed Storage Proteins; Milk Proteins; Egg Proteins, Dietary; Glycoside Hydrolases
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-02-26
Route ORAL
Dosage form LIQUID
Substance POTASSIUM GLUCONATE; SUS SCROFA ADRENAL GLAND; PORK LIVER; COFFEA ARABICA SEED, ROASTED; GREEN TEA LEAF; ACTIVATED CHARCOAL; FERROUS IODIDE; IRON; GELSEMIUM SEMPERVIRENS ROOT; IODINE; IRIDIUM; LYCOPODIUM CLAVATUM SPORE; PULSATILLA PRATENSIS WHOLE; SELENIU
Why two NDCs? The FDA registers this code as 43742-1950-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 43742-1950-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerDeseret Biologicals, Inc.
Labeler code43742
First marketedFeb 2021
Product typeHuman Otc Drug
Portfolio617 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

Enviro I is an unapproved homeopathic liquid taken by mouth that contains potassium gluconate along with numerous plant, mineral, and animal-derived substances. In homeopathic practice, these ingredients are traditionally used to address various conditions, though homeopathic products are marketed based on traditional use rather than scientific evidence evaluated by the FDA. The product includes common food allergens and extracts believed in homeopathic tradition to support different body systems. Homeopathic remedies are highly diluted preparations and are not proven effective by modern medical standards.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Enviro I 6 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 10 [hp_X]/mL; 10 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mLthis 43742-1950-01 Deseret 30 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2021
On the market since
Feb 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
43742-1950-01 You're viewing this 30 mL in 1 BOTTLE, DROPPER (43742-1950-1) 2021-02-26 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

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 Metal 6 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mL; 10 [hp_X]/mL; 10 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL; 12 [hp_X]/mL LIQUID is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 43742-1950-1, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 43742-1950-01, written without dashes as 43742195001. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 43742-1950-01, the first segment (43742) is the labeler code FDA assigned to Deseret Biologicals, Inc.; the middle segment (1950) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Deseret Biologicals, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Deseret Biologicals, Inc. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 46 words ▾

USES: • For the temporary relief of symptoms including: • sensitivity to food • swelling of lips • stomach cramps • vomiting • occasional diarrhea • skin rash These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

⏱️ Dosage and Administration 29 words ▾

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.

⚠️ Warnings 45 words ▾

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

🧪 Active Ingredient 189 words ▾

ACTIVE INGREDIENTS: Allium Cepa 12X, 30X, Amygdala Amara 12X, 30X, Apple 12X, 30X, Banana 12X, 30X, Beef 12X, 30X, Black Walnut 12X, 30X, Brazil Nut 12X, 30X, Cacao 10C, 12C, 15C, 30C, Carbo Vegetabilis 12X, Cashew 12X, 30X, Cheese 12X, 30X, Chicken 12X, 30X, Coconut 12X, 30X, Cod 12X, 30X, Coffea Tosta 10X, 12X, 15X, 30X, Cortisone Aceticum 30X, Crab 12X, 30X, Egg 12X, 30X, Eggplant 12X, 30X, English Walnut 12X, 30X, Ferrum Iodatum 12X, Ferrum Metallicum 12X, Fragaria Vesca 12X, 30X, Gelsemium Sempervirens 12X, Glandula Suprarenalis Suis 8X, Hepar Suis 8X, Histaminum Hydrochloricum 30X, Hyaluronidase 30X, Interferon 30X, Iodium 12X, Iridium Metallicum 12X, Lac Vaccinum 12X, 30X, Lamb 12X, 30X, Linum Usitatissimum 12X, 30X, Lycopodium Clavatum 12X, Orange 12X, 30X, Oyster 12X, 30X, Peanut 12X, 30X, Pecan 12X, 30X, Phaseolus 12X, 30X, Piper Nigrum 12X, 30X, Pork 12X, 30X, Potassium Gluconate 6X, Pulsatilla (Pratensis) 12X, Rape Seed Oil 12X, 30X, Salmon 12X, 30X, Selenium Metallicum 12X, Serotonin (Hydrochloride) 30X, Sesame Seed 12X, 30X, Shrimp 12X, 30X, Solanum Tuberosum 12X, 30X, Thea Sinensis 10X, 12X, 15X, 30X, Tomato 12X, 30X, Tuna 12X, 30X, Wheat 12X, 30X, Zincum Metallicum 12X.

🧪 Inactive Ingredients 6 words ▾

INACTIVE INGREDIENTS: Demineralized water, 25% ethanol

🎯 Purpose ~1 min read ▾

PURPOSE: Allium Cepa – Sensitivity to Food, Amygdala Amara – Stomach Cramps, Apple – Skin Rash, Banana – Occasional Diarrhea, Beef – Stomach Cramps, Black Walnut - Vomiting, Brazil Nut – Swelling of Lips, Cacao – Occasional Diarrhea, Carbo Vegetabilis – Sensitivity to Food, Cashew – Occasional Diarrhea, Cheese – Stomach Cramps, Chicken – Sensitivity to Food, Coconut – Sensitivity to Food, Cod – Skin Rash, Coffea Tosta – Skin Rash, Cortisone Aceticum – Sensitivity to Food, Crab – Skin Rash, Egg – Stomach Cramps, Eggplant – Stomach Cramps, English Walnut – Occasional Diarrhea, Ferrum Iodatum – Stomach Cramps, Ferrum Metallicum - Vomiting, Fragaria Vesca – Occasional Diarrhea, Gelsemium Sempervirens – Stomach Cramps, Glandula Suprarenalis Suis – Stomach Cramps, Hepar Suis - Vomiting, Histaminum Hydrochloricum – Occasional Diarrhea, Hyaluronidase – Sensitivity to Food, Interferon – Sensitivity to Food, Iodium – Swelling of Lips, Iridium Metallicum – Stomach Cramps, Lac Vaccinum – Sensitivity to Food, Lamb – Swelling of Lips, Linum Usitatissimum – Swelling of Lips, Lycopodium Clavatum - Vomiting, Orange – Occasional Diarrhea, Oyster – Swelling of Lips, Peanut – Sensitivity to Food, Pecan - Swelling of Lips, Phaseolus - Vomiting, Piper Nigrum – Occasional Diarrhea, Pork - Vomiting, Potassium Gluconate – Stomach Cramps, Pulsatilla (Pratensis) – Skin Rash, Rape Seed Oil - Vomiting, Salmon – Sensitivity to Food, Selenium Metallicum – Sensitivity to Food, Serotonin (Hydrochloride) – Sensitivity to Food, Sesame Seed – Swelling of Lips, Shrimp – Swelling of Lips, Solanum Tuberosum - Vomiting, Thea Sinensis – Occasional Diarrhea, Tomato – Stomach Cramps, Tuna – Skin Rash, Wheat – Sensitivity to Food, Zincum Metallicum – Swelling of Lips

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 43742-1949-01 · Deseret 43742-1951-01 · Deseret →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.