NDC 43742-0398 Glucoreg

Ascorbic Acid, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Acetaldehyde, Dhea (dehydroepiandrosterone), Insulinum, Phloridzinum, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Disodium, Citricum Acidum, Coenzyme A, Fumaricum Acidum, Glyoxal Trimer Dihydrate, Nadidum, Hepar Suis, Pancreas Suis, Glucagon, Baryta Oxalica, Alloxanum, Berberis Vulgaris, Carcinosin, Lycopodium Clavatum, Momordica Balsamina, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum,

NDC Product Code 43742-0398

NDC Code: 43742-0398

Proprietary Name: Glucoreg 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: Ascorbic Acid, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Acetaldehyde, Dhea (dehydroepiandrosterone), Insulinum, Phloridzinum, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Disodium, Citricum Acidum, Coenzyme A, Fumaricum Acidum, Glyoxal Trimer Dihydrate, Nadidum, Hepar Suis, Pancreas Suis, Glucagon, Baryta Oxalica, Alloxanum, Berberis Vulgaris, Carcinosin, Lycopodium Clavatum, Momordica Balsamina, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, 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.
    • 43742-0398 - Glucoreg

NDC 43742-0398-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Glucoreg with NDC 43742-0398 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Glucoreg is ascorbic acid, pyridoxinum hydrochloricum, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, acetaldehyde, dhea (dehydroepiandrosterone), insulinum, phloridzinum, alpha-lipoicum acidum, adenosinum triphosphoricum disodium, citricum acidum, coenzyme a, fumaricum acidum, glyoxal trimer dihydrate, nadidum, hepar suis, pancreas suis, glucagon, baryta oxalica, alloxanum, berberis vulgaris, carcinosin, lycopodium clavatum, momordica balsamina, phosphoricum acidum, phosphorus, syzygium jambolanum,. 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.

Glucoreg 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.

  • ASCORBIC ACID 6 [hp_X]/mL
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL
  • RIBOFLAVIN 6 [hp_X]/mL
  • LACTIC ACID, L- 6 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • ACETALDEHYDE 6 [hp_X]/mL
  • PRASTERONE 6 [hp_X]/mL
  • INSULIN PORK 6 [hp_X]/mL
  • PHLORIZIN 6 [hp_X]/mL
  • THIOCTIC ACID 8 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 8 [hp_X]/mL
  • ANHYDROUS CITRIC ACID 8 [hp_X]/mL
  • COENZYME A 8 [hp_X]/mL
  • FUMARIC ACID 8 [hp_X]/mL
  • GLYOXAL 8 [hp_X]/mL
  • NADIDE 8 [hp_X]/mL
  • PORK LIVER 10 [hp_X]/mL
  • SUS SCROFA PANCREAS 10 [hp_X]/mL
  • GLUCAGON 12 [hp_X]/mL
  • BARIUM OXALATE 6 [hp_C]/mL
  • ALLOXAN 6 [hp_C]/mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_C]/mL
  • HUMAN BREAST TUMOR CELL 6 [hp_C]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_C]/mL
  • MOMORDICA BALSAMINA IMMATURE FRUIT 6 [hp_C]/mL
  • PHOSPHORIC ACID 6 [hp_C]/mL
  • PHOSPHORUS 6 [hp_C]/mL
  • SYZYGIUM CUMINI SEED 6 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • GYMNEMA SYLVESTRE LEAF 30 [hp_C]/mL
  • FENUGREEK SEED 30 [hp_C]/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: 04-23-2014 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: 11-26-2019 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.

Glucoreg Product Label Images

Glucoreg 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:

Ascorbic Acid 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Sarcolacticum Acidum 6X, Thiaminum Hydrochloricum 6X, Acetaldehyde 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, DHEA (Dehydroepiandrosterone) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Insulinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Phloridzinum 6X, 30X, 200X, 12C, 30C, 60C, 200C, alpha-Lipoicum Acidum 8X, Adenosinum Triphosphoricum Disodium 8X, Citricum Acidum 8X, Coenzyme A 8X, Fumaricum Acidum 8X, Glyoxal Trimer Dihydrate 8X, Nadidum 8X, Hepar Suis 10X, Pancreas Suis 10X, Glucagon 12X, 30X, 200X, 12C, 30C, 60C, 200C, Baryta Oxalica 6C, Alloxanum 6C, 30C, Berberis Vulgaris 6X, 30X, 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.

Indications:

For temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.

For temporary relief of symptoms related to high blood sugar including dry mouth, thirst, excess urination, night sweats, sugar and carb cravings.

Warnings:

Keep out of reach of children.  In case of overdose, get medical help or contact 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, get medical help or contact 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:

Distributed by Deseret Biologicals, Inc.469 W. Parkland Drive, Sandy, UT 84070www.desbio.com

Package Label Display:

DESBIONDC 43742-0398-1HOMEOPATHICGLUCOREG1 FL OZ (30 ml)

* Please review the disclaimer below.

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