NDC 43742-0808 Emf Protect And Balance

Alfalfa, Laminaria Digitata, Symphytum Officinale, Ascorbic Acid, Melatonin, Calcarea Carbonica, Cuprum Metallicum, Ferrum Metallicum, Iodium, Manganum Aceticum, Silicea, Phosphorus, Magnetis Polus Arcticus, Magnetis Polus Australis, X-ray, Agate, Quartz, Carbon Dioxide, Aconitum Napellus, Arsenicum Album, Gaertner Bacillus (bach), Kali Carbonicum

NDC Product Code 43742-0808

NDC CODE: 43742-0808

Proprietary Name: Emf Protect And Balance 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: Alfalfa, Laminaria Digitata, Symphytum Officinale, Ascorbic Acid, Melatonin, Calcarea Carbonica, Cuprum Metallicum, Ferrum Metallicum, Iodium, Manganum Aceticum, Silicea, Phosphorus, Magnetis Polus Arcticus, Magnetis Polus Australis, X-ray, Agate, Quartz, Carbon Dioxide, Aconitum Napellus, Arsenicum Album, Gaertner Bacillus (bach), Kali Carbonicum 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
  • Melatonin has been used for short-term treatment of trouble sleeping (insomnia) due to sleep cycle disorders and time changes (jet lag). This product may help you fall asleep faster and decrease the number of times you awaken during the night. It may also help you sleep for a longer time. Melatonin is a substance that your body normally makes. It is thought to help your body's regular daily cycle, hormone production, and sleep patterns. Some herbal/diet supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details regarding the particular brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.
  • Drug uses not available
  • This medication is an iron supplement used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy). Iron is an important mineral that the body needs to produce red blood cells and keep you in good health.
  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0808-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Emf Protect And Balance with NDC 43742-0808 is a a human prescription drug product labeled by Deseret Biologicals, Inc.. The generic name of Emf Protect And Balance is alfalfa, laminaria digitata, symphytum officinale, ascorbic acid, melatonin, calcarea carbonica, cuprum metallicum, ferrum metallicum, iodium, manganum aceticum, silicea, phosphorus, magnetis polus arcticus, magnetis polus australis, x-ray, agate, quartz, carbon dioxide, aconitum napellus, arsenicum album, gaertner bacillus (bach), kali carbonicum. 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 Prescription 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.

Emf Protect And Balance 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.

  • ALFALFA 3 [hp_X]/mL
  • LAMINARIA DIGITATA 3 [hp_X]/mL
  • COMFREY ROOT 6 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • MELATONIN 6 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • COPPER 8 [hp_X]/mL
  • IRON 8 [hp_X]/mL
  • IODINE 8 [hp_X]/mL
  • MANGANESE ACETATE TETRAHYDRATE 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • PHOSPHORUS 8 [hp_X]/mL
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) 8 [hp_X]/mL
  • CARBON DIOXIDE 30 [hp_X]/mL
  • ACONITUM NAPELLUS 30 [hp_C]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • POTASSIUM CARBONATE 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.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Radiographic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • X-Ray Contrast Activity - [MoA] (Mechanism of Action)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
  • Ascorbic Acid - [CS]

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: 07-12-2016 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: 08-16-2021 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.

Emf Protect And Balance 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:

Alfalfa 3X, Laminaria Digitata 3X, Symphytum Officinale 6X, Ascorbic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Melatonin 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Calcarea Carbonica 8X, Cuprum Metallicum 8X, Ferrum Metallicum 8X, Iodium 8X, Manganum Aceticum 8X, Silicea 8X, Phosphorus 8X, 30X, Magnetis Polus Arcticus 8X, 30X, 60X, 100X, 200X Magnetis Polus Australis 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, X-Ray 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Agate 12X, Quartz 12X, Carbon Dioxide 30X, 60X, 200X, Aconitum Napellus 30C, Arsenicum Album 30C, Gaertner Bacillus (Bach) 30C, Kali Carbonicum 30C.

Homeopathic Indications:

For temporary relief of symptoms related to Jet Lag, general body aches, nervousness, muscle cramps, sleep dysfunction, and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to Jet Lag, general body aches, nervousness, muscle cramps, sleep dysfunction, and fatigue.****These statements are based upon traditional 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 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 physician or 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:

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

Package Label Display:

DESBIONDC 43742-0808-1HOMEOPATHICEMT PROTECT AND BALANCE1 FL OZ (30 ml)

* Please review the disclaimer below.