NDC 43742-0380 Governing Vessel Conception Vessel Meridian Formula

Phenylalanine, Taurine, Nerve (suis), Ascorbic Acid, Adenosinum Triphosphoricum Dinatrum, Brain (suis), Sarcolacticum Acidum, Adrenocorticotrophin, Malvin, Apis Mellifica, Arsenicum Album, Baryta Carbonica, Belladonna, Calcarea Carbonica, Cicuta Virosa, Conium Maculatum, Ferrum Metallicum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Phosphorus, Pulsatilla (vulgaris), Sepia, Tarentula Hispana, Thuja Occidentalis, Dysentery Bacillus

NDC Product Code 43742-0380

NDC Code: 43742-0380

Proprietary Name: Governing Vessel Conception Vessel Meridian Formula 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: Phenylalanine, Taurine, Nerve (suis), Ascorbic Acid, Adenosinum Triphosphoricum Dinatrum, Brain (suis), Sarcolacticum Acidum, Adrenocorticotrophin, Malvin, Apis Mellifica, Arsenicum Album, Baryta Carbonica, Belladonna, Calcarea Carbonica, Cicuta Virosa, Conium Maculatum, Ferrum Metallicum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Phosphorus, Pulsatilla (vulgaris), Sepia, Tarentula Hispana, Thuja Occidentalis, Dysentery Bacillus 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.
    • 43742-0380 - Governing Vessel Conception Vessel

NDC 43742-0380-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Governing Vessel Conception Vessel Meridian Formula with NDC 43742-0380 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Governing Vessel Conception Vessel Meridian Formula is phenylalanine, taurine, nerve (suis), ascorbic acid, adenosinum triphosphoricum dinatrum, brain (suis), sarcolacticum acidum, adrenocorticotrophin, malvin, apis mellifica, arsenicum album, baryta carbonica, belladonna, calcarea carbonica, cicuta virosa, conium maculatum, ferrum metallicum, lachesis mutus, lycopodium clavatum, mercurius solubilis, natrum sulphuricum, phosphorus, pulsatilla (vulgaris), sepia, tarentula hispana, thuja occidentalis, dysentery bacillus. 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.

Governing Vessel Conception Vessel Meridian Formula 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.

  • PHENYLALANINE 6 [hp_X]/mL
  • TAURINE 6 [hp_X]/mL
  • SUS SCROFA NERVE 8 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_C]/mL
  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_C]/mL
  • PORK BRAIN 6 [hp_C]/mL
  • LACTIC ACID, L- 6 [hp_C]/mL
  • CORTICOTROPIN 8 [hp_C]/mL
  • MALVIN 10 [hp_C]/mL
  • APIS MELLIFERA 30 [hp_C]/mL
  • ARSENIC ACID 30 [hp_C]/mL
  • BARIUM CARBONATE 30 [hp_C]/mL
  • ATROPA BELLADONNA 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
  • CICUTA VIROSA ROOT 30 [hp_C]/mL
  • CONIUM MACULATUM FLOWERING TOP 30 [hp_C]/mL
  • IRON 30 [hp_C]/mL
  • LACHESIS MUTA VENOM 30 [hp_C]/mL
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
  • MERCURIUS SOLUBILIS 30 [hp_C]/mL
  • SODIUM SULFATE 30 [hp_C]/mL
  • PHOSPHORUS 30 [hp_C]/mL
  • PULSATILLA VULGARIS 30 [hp_C]/mL
  • SEPIA OFFICINALIS JUICE 30 [hp_C]/mL
  • LYCOSA TARANTULA 30 [hp_C]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 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: 06-13-2014 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: 08-19-2020 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.

Governing Vessel Conception Vessel Meridian Formula Product Label Images

Governing Vessel Conception Vessel Meridian Formula 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:

Phenylalanine 6X, 10X, 30X, 200X, Taurine 6X, 8X, 10X, 30X, 200X, Nerve (Suis) 8X, Adenosinum Triphosphoricum Dinatrum 6C, 30C, Ascorbic Acid 6C, 30C, Brain (Suis) 6C, 30C, Sarcolacticum Acidum 6C, 30C, Adrenocorticotrophin 8C, 30C, Malvin 10C, 15C, 100C, Apis Mellifica 30C, Arsenicum Album 30C, Baryta Carbonica 30C, Belladonna 30C, Calcarea Carbonica 30C, Cicuta Virosa 30C, Conium Maculatum 30C, Ferrum Metallicum 30C, Lachesis Mutus 30C, Lycopodium Clavatum 30C, Mercurius Solubilis 30C, Natrum Sulphuricum 30C, Phosphorus 30C, Pulsatilla (Vulgaris) 30C, Sepia 30C, Tarentula Hispana 30C, Thuja Occidentalis 30C, Dysentery Bacillus 30C, 200C.

Indications:

Temporary relief of symptoms related to blocked energy in the body including fatigue, temperature fluctuations, cramping and nervousness.

Temporary relief of symptoms related to blocked energy in the body including fatigue, temperature fluctuations, cramping and nervousness.

Warnings:

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult a health professional before use.Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store at room temperature.Keep out of direct sunlight.

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:

Adults 3 to 10 drops under the tongue 3 times daily or as directed by your 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., Sandy, UT 84070800.827.9529    www.desbio.com

Package Label Display:

NAMIBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0380-1GOVERNING VESSEL CONCEPTION VESSELMeridian FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.

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