NDC 43742-0656 Bio Cytotox Phase

Colchicum Autumnale, Conium Maculatum, Hydrastis Canadensis, Vaccinium Myrtillus, Podophyllum Peltatum, Ascorbic Acid, Galium Aparine, Nicotinamidum, Pyridoxinum Hydrochloricum, Norepinephrine, Alpha-lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthraquinone, Coenzyme A, Histaminum Hydrochloricum, Magnesium Gluconate, Nadidum, Naphthoquinone, Ubidecarenonum, Manganum Phosphoricum, Hydroquinone, Morgan Gaertner

NDC Product Code 43742-0656

NDC Code: 43742-0656

Proprietary Name: Bio Cytotox 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: Colchicum Autumnale, Conium Maculatum, Hydrastis Canadensis, Vaccinium Myrtillus, Podophyllum Peltatum, Ascorbic Acid, Galium Aparine, Nicotinamidum, Pyridoxinum Hydrochloricum, Norepinephrine, Alpha-lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthraquinone, Coenzyme A, Histaminum Hydrochloricum, Magnesium Gluconate, Nadidum, Naphthoquinone, Ubidecarenonum, Manganum Phosphoricum, Hydroquinone, Morgan Gaertner 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.
    • 43742-0656 - Bio Cytotox Phase

NDC 43742-0656-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio Cytotox Phase with NDC 43742-0656 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Bio Cytotox Phase is colchicum autumnale, conium maculatum, hydrastis canadensis, vaccinium myrtillus, podophyllum peltatum, ascorbic acid, galium aparine, nicotinamidum, pyridoxinum hydrochloricum, norepinephrine, alpha-lipoicum acidum, natrum oxalaceticum, sulphur, acetylsalicylicum acidum, adenosinum triphosphoricum dinatrum, anthraquinone, coenzyme a, histaminum hydrochloricum, magnesium gluconate, nadidum, naphthoquinone, ubidecarenonum, manganum phosphoricum, hydroquinone, morgan gaertner. 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.

Bio Cytotox 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.

  • COLCHICUM AUTUMNALE BULB 4 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 4 [hp_X]/mL
  • GOLDENSEAL 4 [hp_X]/mL
  • BILBERRY 4 [hp_X]/mL
  • PODOPHYLLUM 5 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • GALIUM APARINE 6 [hp_X]/mL
  • NIACINAMIDE 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
  • NOREPINEPHRINE 6 [hp_X]/mL
  • THIOCTIC ACID 8 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • ASPIRIN 10 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
  • ANTHRAQUINONE 10 [hp_X]/mL
  • COENZYME A 10 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/mL
  • MAGNESIUM GLUCONATE 10 [hp_X]/mL
  • NADIDE 10 [hp_X]/mL
  • NAPHTHOQUINE 10 [hp_X]/mL
  • UBIDECARENONE 10 [hp_X]/mL
  • MANGANESE PYROPHOSPHATE 15 [hp_X]/mL
  • HYDROQUINONE 3 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 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: 11-11-2015 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: 12-17-2020 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 Cytotox Phase Product Label Images

Bio Cytotox 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:

Colchicum Autumnale 4X, Conium Maculatum 4X, Hydrastis Canadensis 4X, Vaccinium Myrtillus 4X, Podophyllum Peltatum 5X, Ascorbic Acid 6X, Galium Aparine 6X, Nicotinamidum 6X, Pyridoxinum Hydrochloricum 6X, Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Alpha-Lipoicum Acidum 8X, Natrum Oxalaceticum 8X, Sulphur 8X, Acetylsalicylicum Acidum10X, Adenosinum Triphosphoricum Dinatrum 10X, Anthraquinone 10X, Coenzyme A 10X, Histaminum Hydrochloricum 10X, Magnesium Gluconate 10X, Nadidum 10X, Naphthoquinone 10X, Ubidecarenonum 10X, Manganum Phosphoricum 15X, Hydroquinone 3C, Morgan Gaertner 30C

Homeopathic Indications:

For the temporary relief of symptoms of fatigue, effects of toxin buildup, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles.  They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms of fatigue, effects of toxin buildup, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away.If pregnant of breast-feeding, seek advice of 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 physician or a 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

Quesitons:

Dist. By:Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070www.desbio.com

Package Label Display:

DESBIONDC 43742-0656-1HOMEOPATHICBIO CYTOTOX PHASE1 FL OZ (30 ml)

* Please review the disclaimer below.

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