Governing Vessel Conception Vessel Meridian Opener

Apis Mellifica, Arsenicum Album, Baryta Carbonica, Calcarea Carbonica, Cicuta Virosa, Conium Maculatum, Ferrum Metallicum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Phosphorus, Pulsatilla (vulgaris), Sepia, Tarentula Hispana, Thuja Occidentalis

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1011

Governing Vessel Conception Vessel Meridian Opener also known as Apis Mellifica, Arsenicum Album, Baryta Carbonica, Calcarea Carbonica, Cicuta Virosa, Conium Maculatum, Ferrum Metallicum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Phosphorus, Pulsatilla (vulgaris), Sepia, Tarentula Hispana, Thuja Occidentalis is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Governing Vessel Conception Vessel Meridian Opener is 43742-1011. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Governing Vessel Conception Vessel Meridian Opener drug includes Apis Mellifera - 30 [hp_C]/mL Arsenic Trioxide - 30 [hp_C]/mL Barium Carbonate - 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 Lycosa Tarantula - 30 [hp_C]/mL Mercurius Solubilis - 30 [hp_C]/mL and more. The currest status of Governing Vessel Conception Vessel Meridian Opener drug is Active.

Drug Information:

Drug NDC:	43742-1011
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Governing Vessel Conception Vessel Meridian Opener
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Apis Mellifica, Arsenicum Album, Baryta Carbonica, Calcarea Carbonica, Cicuta Virosa, Conium Maculatum, Ferrum Metallicum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Solubilis, Natrum Sulphuricum, Phosphorus, Pulsatilla (vulgaris), Sepia, Tarentula Hispana, Thuja Occidentalis
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	APIS MELLIFERA - 30 [hp_C]/mL ARSENIC TRIOXIDE - 30 [hp_C]/mL BARIUM CARBONATE - 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 LYCOSA TARANTULA - 30 [hp_C]/mL MERCURIUS SOLUBILIS - 30 [hp_C]/mL Load more... OYSTER SHELL CALCIUM CARBONATE, CRUDE - 30 [hp_C]/mL PHOSPHORUS - 30 [hp_C]/mL PULSATILLA VULGARIS - 30 [hp_C]/mL SEPIA OFFICINALIS JUICE - 30 [hp_C]/mL SODIUM SULFATE - 30 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG - 30 [hp_C]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	15 May, 2017
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	19 Jul, 2023
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.
Listing Expiration Date:	23 Dec, 2025
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	7S82P3R43Z S7V92P67HO 6P669D8HQ8 YEA9P21S8N Q28R5GF371 E1UOL152H7 VSW71SS07I C88X29Y479 86M454L2TT 324Y4038G2 Load more... 2E32821G6I 27YLU75U4W I76KB35JEV QDL83WN8C2 0YPR65R21J 1NT28V9397
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Bee Venoms [CS] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Standardized Insect Venom Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1011-1	30 mL in 1 BOTTLE, DROPPER (43742-1011-1)	15 May, 2017	19 Jul, 2023	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Governing Vessel Conception Vessel Meridian Opener

Apis Mellifica & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1011

Purpose:

Homeopathic indications: for temporary relief of symptoms such as poor digestion, bloating and stress.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Governing vessel conception vessel meridian opener apis mellifica, arsenicum album, baryta carbonica, calcarea carbonica, cicuta virosa, conium maculatum, ferrum metallicum, lachesis mutus, lycopodium clavatum, mercurius solubilis, natrum sulphuricum, phosphorus, pulsatilla (vulgaris), sepia, tarentula hispana, thuja occidentalis apis mellifera apis mellifera arsenic trioxide arsenic cation (3+) barium carbonate barium cation oyster shell calcium carbonate, crude oyster shell calcium carbonate, crude cicuta virosa root cicuta virosa root conium maculatum flowering top conium maculatum flowering top iron iron lachesis muta venom lachesis muta venom lycopodium clavatum spore lycopodium clavatum spore mercurius solubilis mercurius solubilis sodium sulfate sodium sulfate anhydrous phosphorus phosphorus pulsatilla vulgaris anemone pulsatilla sepia officinalis juice sepia officinalis juice lycosa tarantula lycosa tarantula thuja occidentalis leafy twig thuja occidentalis leafy twig water alcohol

Indications and Usage:

Warnings:

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.

Dosage and Administration:

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.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-0828-1 homeopathic governing vessel conception vessel meridian opener 1 fl oz (30 ml) governing vessel conception vessel meridian opener

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.