NDC 43742-0402 Bio Co-enzyme Phase

Beta Vulgaris, Ascorbic Acid, Cysteinum, Natrum Oxalaceticum, Nicotinamidum, Pulsatilla (vulgaris), Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Adrenalinum, Alpha-ketoglutaricum Acidum, Alpha-lipoicum Acidum, Cerium Oxalicum, Cis-aconitic Acid, Citricum Acidum, Coenzyme A, Fumaricum Acidum, Magnesium Orotate, Malic Acid, Nadidum, Natrum Pyruvicum, Succinicum Acidum, Adenosinum Triphosphoricum Dinatrum, Hepar Sulphuris Calcareum, Sulphur, Manganum Phosphoricum, Baryta Oxalsuccinicum

NDC Product Code 43742-0402

NDC Code: 43742-0402

Proprietary Name: Bio Co-enzyme Phase 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: Beta Vulgaris, Ascorbic Acid, Cysteinum, Natrum Oxalaceticum, Nicotinamidum, Pulsatilla (vulgaris), Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Adrenalinum, Alpha-ketoglutaricum Acidum, Alpha-lipoicum Acidum, Cerium Oxalicum, Cis-aconitic Acid, Citricum Acidum, Coenzyme A, Fumaricum Acidum, Magnesium Orotate, Malic Acid, Nadidum, Natrum Pyruvicum, Succinicum Acidum, Adenosinum Triphosphoricum Dinatrum, Hepar Sulphuris Calcareum, Sulphur, Manganum Phosphoricum, Baryta Oxalsuccinicum 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 Biolgicals, Inc.
    • 43742-0402 - Bio Co-enzyme Phase

NDC 43742-0402-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio Co-enzyme Phase with NDC 43742-0402 is a a human over the counter drug product labeled by Deseret Biolgicals, Inc.. The generic name of Bio Co-enzyme Phase is beta vulgaris, ascorbic acid, cysteinum, natrum oxalaceticum, nicotinamidum, pulsatilla (vulgaris), pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, adrenalinum, alpha-ketoglutaricum acidum, alpha-lipoicum acidum, cerium oxalicum, cis-aconitic acid, citricum acidum, coenzyme a, fumaricum acidum, magnesium orotate, malic acid, nadidum, natrum pyruvicum, succinicum acidum, adenosinum triphosphoricum dinatrum, hepar sulphuris calcareum, sulphur, manganum phosphoricum, baryta oxalsuccinicum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biolgicals, 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.

Bio Co-enzyme Phase 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.

  • BETA VULGARIS 4 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • CYSTEINE 6 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
  • NIACINAMIDE 6 [hp_X]/mL
  • PULSATILLA VULGARIS 6 [hp_X]/mL
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL
  • RIBOFLAVIN 6 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • EPINEPHRINE 6 [hp_X]/mL
  • OXOGLURIC ACID 8 [hp_X]/mL
  • THIOCTIC ACID 8 [hp_X]/mL
  • CEROUS OXALATE NONAHYDRATE 8 [hp_X]/mL
  • ACONITIC ACID, (Z)- 8 [hp_X]/mL
  • ANHYDROUS CITRIC ACID 8 [hp_X]/mL
  • COENZYME A 8 [hp_X]/mL
  • FUMARIC ACID 8 [hp_X]/mL
  • MAGNESIUM OROTATE 8 [hp_X]/mL
  • MALIC ACID 8 [hp_X]/mL
  • NADIDE 8 [hp_X]/mL
  • SODIUM PYRUVATE 8 1/mL
  • SUCCINIC ACID 8 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
  • CALCIUM SULFIDE 10 1/mL
  • SULFUR 10 [hp_X]/mL
  • MANGANESE PHOSPHATE, DIBASIC 16 [hp_X]/mL
  • BARIUM OXALOSUCCINATE 30 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_X]/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 Biolgicals, 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: 03-31-2014 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: 11-16-2020 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.

Bio Co-enzyme Phase 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:

Beta Vulgaris 4X, Ascorbic Acid 6X, Cysteinum 6X, Natrum Oxalaceticum 6X, Nicotinamidum 6X, Pulsatilla (Vulgaris) 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Thiaminum Hydrochloricum 6X, Adrenalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, alpha-Ketoglutaricum Acidum 8X, alpha-Lipoicum Acidum 8X, Cerium Oxalicum 8X, CIS-Aconitic Acid 8X, Citricum Acidum 8X, Coenzyme A 8X, Fumaricum Acidum 8X, Magnesium Orotate 8X, Malic Acid 8X, Nadidum 8X, Natrum Pyruvicum 8X, Succinicum Acidum 8X, Adenosinum Triphosphoricum Dinatrum 10X, Hepar Sulphuris Calcareum 10X, Sulphur 10X, Manganum Phosphoricum 16X, Baryta Oxalsuccinicum 30C, Morgan Bacillus (Pure) 30C

Homeopathic Indications:

For the temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of exhaustion, fatigue, and feelings of low energy.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

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.

Keep Out Of Reach Of Children:

Keep out of reach of children.  In case of overdose, contact a physician or Poison Control Center right away.

Directions:

1-10 drops under the tongue, 2 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 43742-0402-1BIO CO-ENZYME PHASE1 FL OZ  (30 ml)

* Please review the disclaimer below.

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