NDC 43742-0401 Bio Cytotox Phase

Colchicum Autumnale, Conium Maculatum, Hydrastis Canadensis, Vaccinium Myrtillus, Podophyllum Peltatum, Ascorbic Acid, Galium Aparine, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Norepinephrine, Alpha-lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Anthraquinone, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Co-enzyme Q-10, Histaminum Hydrochloricum, Magnesium Gluconate, Nadidum, Naphthoquinone, Manganum Phosphoricum,

NDC Product Code 43742-0401

NDC CODE: 43742-0401

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, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Norepinephrine, Alpha-lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Anthraquinone, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Co-enzyme Q-10, Histaminum Hydrochloricum, Magnesium Gluconate, Nadidum, Naphthoquinone, Manganum Phosphoricum, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • Niacinamide (nicotinamide) is a form of vitamin B3 (niacin) and is used to prevent and treat niacin deficiency (pellagra). Niacin deficiency can cause diarrhea, confusion (dementia), tongue redness/swelling, and peeling red skin. Niacinamide is often used instead of niacin because it causes fewer side effects (e.g., flushing). Unlike niacin, niacinamide does not help correct blood fat levels and cannot be substituted for niacin if you are being treated for a blood fat problem (e.g., high cholesterol). Niacin deficiency may happen as a result of poor diet, certain medical conditions (e.g., alcohol abuse, malabsorption syndrome, Hartnup disease), or long-term use of certain medications (e.g., isoniazid). It is best to get your vitamins from healthy foods. A multivitamin may be recommended by your doctor instead of niacinamide because poor diet usually causes deficiencies in more than one vitamin. Vitamins help to support the body's ability to make and break down natural substances (metabolism) and are needed for good health.
  • Aspirin is used to reduce fever and relieve mild to moderate pain from conditions such as muscle aches, toothaches, common cold, and headaches. It may also be used to reduce pain and swelling in conditions such as arthritis. Aspirin is known as a salicylate and a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking a certain natural substance in your body to reduce pain and swelling. Consult your doctor before treating a child younger than 12 years. Your doctor may direct you to take a low dose of aspirin to prevent blood clots. This effect reduces the risk of stroke and heart attack. If you have recently had surgery on clogged arteries (such as bypass surgery, carotid endarterectomy, coronary stent), your doctor may direct you to use aspirin in low doses as a blood thinner to prevent blood clots.
  • Coenzyme Q10 has been used for heart problems (e.g., heart failure, angina), high blood pressure, Parkinson's disease, gum disease, and certain diseases passed down through families (Huntington's disease, muscular dystrophy). It has also been used for reducing the number of migraine headaches and for reducing cell damage that may occur after surgery or treatment with certain anti-cancer drugs. If you have or think you have any of the conditions listed above, consult your doctor for advice on proper care and treatment. Coenzyme Q10 is a substance that your body normally makes. Your body uses it to help keep in good health. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
  • This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with water pills (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).
  • Hydroquinone is used to lighten the dark patches of skin (also called hyperpigmentation, melasma, liver spots, age spots, freckles) caused by pregnancy, birth control pills, hormone medicine, or injury to the skin. This medicine works by blocking the process in the skin that leads to discoloration.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0401-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bio Cytotox Phase with NDC 43742-0401 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, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, norepinephrine, alpha-lipoicum acidum, natrum oxalaceticum, sulphur, acetylsalicylicum acidum, anthraquinone, adenosinum triphosphoricum dinatrum, coenzyme a, co-enzyme q-10, histaminum hydrochloricum, magnesium gluconate, nadidum, naphthoquinone, manganum phosphoricum, . 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
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • ASPIRIN 10 [hp_X]/mL
  • ANTHRAQUINONE 10 [hp_X]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
  • COENZYME A 10 [hp_X]/mL
  • UBIDECARENONE 10 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/mL
  • MAGNESIUM GLUCONATE 10 [hp_X]/mL
  • NADIDE 10 [hp_X]/mL
  • 1,4-NAPHTHOQUINONE 10 [hp_X]/mL
  • MANGANESE PHOSPHATE, DIBASIC 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.
  • 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: 09-11-2014 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: 07-22-2020 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’.

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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, Riboflavinum 6X, Sarcolacticum Acidum 6X, Thiaminum Hydrochloricum 6X, Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, alpha-Lipoicum Acidum 8X, Natrum Oxalaceticum 8X, Sulphur 8X, Acetylsalicylicum Acidum 10X, Anthraquinone 10X, Adenosinum Triphosphoricum Dinatrum 10X, Coenzyme A 10X, Ubidecarenonum 10X, Histaminum Hydrochloricum 10X, Magnesium Gluconate 10X, Nadidum 10X, Naphthoquinone 10X, Manganum Phosphoricum 15X, Hydroquinone 3C, Morgan Gaertner 30C.

Indications:

For the temporary relief of symptoms of chronic illness including fatigue, effects of toxin buildup, slowed metabolism, and weakened constitution.

For the temporary relief of symptoms of chronic illness including fatigue, effects of toxin buildup, slowed metabolism, and weakened constitution.

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 43742-0401-1HOMEOPATHICBIO CYTOTOXPHASE1 FL OZ (30 ml)

* Please review the disclaimer below.