NDC 43742-1566-01 — Glucoreg Ascorbicum Acidum, Pyridoxinum

🆔 Identity & classification

FDA NDC (as labeled) 43742-1566-1

Product NDC 43742-1566

11-digit billing NDC 43742156601

UNII PQ6CK8PD0R, 68Y4CF58BV, TLM2976OFR, F9S9FFU82N, M572600E5P, 459AG36T1B +12 more

SPL Set ID 5117f980-95b8-4fc8-9425-8f6f05639437

Established class (EPC) Vitamin C; Calculi Dissolution Agent; Anti-coagulant; Insulin

Mechanism of action Acidifying Activity; Calcium Chelating Activity

Physiologic effect Decreased Coagulation Factor Activity

Chemical class Ascorbic Acid; Insulin

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2019-09-24

Marketing end 2027-07-12

Route ORAL

Dosage form LIQUID

Substance ASCORBIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; LACTIC ACID, L-; THIAMINE HYDROCHLORIDE; PRASTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; THIOCTIC ACID; ANHYDROUS CITRIC ACID; FUMARIC ACID; NADIDE; PANTOTHENIC ACID; ACETALDEHYDE; INSULIN PORK; PORK LIVER

Why two NDCs? The FDA registers this code as 43742-1566-1 — 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 → 43742-1566-01. 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 marketedSep 2019

Product typeHuman Otc Drug

Portfolio617 products on file

🔎 All NDCs from Deseret Biologicals, Inc.

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?

Glucoreg Ascorbicum is an unapproved homeopathic liquid taken by mouth that contains multiple ingredients traditionally used in homeopathic practice. The product includes vitamins like ascorbic acid (vitamin C), thiamine, and riboflavin, along with substances such as insulin, lactic acid, and plant extracts like Berberis vulgaris and Gymnema sylvestre. Homeopathic products are marketed based on homeopathic tradition rather than FDA evaluation for safety or effectiveness. This listing should not be interpreted as medical advice or evidence that the product is proven to treat any condition.

Patient education

📘 MedlinePlus patient leaflet ↗

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 system	Per mL	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Glucoreg 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 8 [hp_X]/mL; 8 [hp_X]/mLthis 43742-1566-01	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

🏛️

2019

On the market since

Sep 2019

📍

2026

Currently FDA-listed

7 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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Glucoreg (this brand).

Top reported reactions

Inflammation1

Reporter sex

Male · 100%

Where does this data come from?

Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
43742-1566-01 You're viewing this	30 mL in 1 BOTTLE, DROPPER (43742-1566-1)	2019-09-24	Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Glucoreg Ascorbicum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, DHEA (Dehydroepiandrosterone), Phloridzinum, Adenosinum Triphosphoricum Dinatrum, alpha-Lipoicum Acidum, Citricum Acidum, Fumaricum Acidum, Nadidu 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 6 [hp_X]/mL; 8 [hp_X]/mL; 8 [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	✓ Available
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 43742-1566-1, 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: 43742-1566-01, written without dashes as 43742156601. 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 43742-1566-01, the first segment (43742) is the labeler code FDA assigned to Deseret Biologicals, Inc.; the middle segment (1566) 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 it is currently marketed — but Deseret Biologicals, Inc. has reported a marketing end date of 2027-07-12, after which this package is expected to stop being marketed. 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 41 words ▾

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to high blood sugar including dry mouth, thirst, night sweats, sugar and carb cravings.** **These statements are based upon traditional 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: 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.

🧪 Active Ingredient 126 words ▾

ACTIVE INGREDIENTS: Ascorbic Acid 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Sarcolacticum Acidum 6X, Thiaminum Hydrochloricum 6X, DHEA (Dehydroepiandrosterone) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Triphosphoricum Dinatrum 8X, alpha-Lipoicum Acidum 8X, Citricum Acidum 8X, Fumaricum Acidum 8X, Nadidum 8X, Pantothenic Acid 8X, Acetaldehyde 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Insulinum (Suis) 8X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Insulinum (Human) 12C, 30C, 60C, 200C, Hepar Suis 10X, Pancreas Suis 10X, Phloridzinum 16X, 24X, 30X, 200X, 12C, 30C, 60C, 200C, Baryta Oxalica 6C, Alloxanum 6C, 30C, Berberis Vulgaris 6C, 30C, Carcinosin 6C, 30C, Lycopodium Clavatum 6C, 30C, Momordica Balsamina 6C, 30C, Phosphoricum Acidum 6C, 30C, Phosphorus 6C, 30C, Syzygium Jambolanum 6C, 30C, Gaertner Bacillus (Bach) 30C, Gymnema Sylvestre 30C, Trigonella Foenum-Graecum 30C.

🧪 Inactive Ingredients 6 words ▾

INACTIVE INGREDIENTS: Demineralized Water, 25% Ethanol

🎯 Purpose 41 words ▾

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to high blood sugar including dry mouth, thirst, night sweats, sugar and carb cravings.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

🔗 Related NDC lookups

🧪 All Ascorbicum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Dhea (Dehydroepiandrosterone), Phloridzinum, Adenosinum Triphosphoricum Dinatrum, Alpha-Lipoicum Acidum, Citricum Acidum, Fumaricum Acidum, Nadidu NDCsSame ingredient 🏭 All Deseret labeler NDCsLabeler code 43742 📚 All Anti-coagulant NDCsDrug class