Aller Balance

Choline Chloride, Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Epinephrine, Onion, Ammonium Carbonate, Apis Mellifera, Arsenic Trioxide, Histamine, Interferon Gamma-1a, Interleukin-12 Human, Manganese Gluconate, Luffa Operculata Fruit, Sus Scrofa Lung, Beef Lung, Sus Scrofa Nasal Mucosa, Bos Taurus Nasal Mucosa, Sodium Chloride, Bos Taurus Peyers Patch, Sus Scrofa Peyers Patch, Schoenocaulon Officinale Seed, Serotonin, Bos Taurus Thymus, Sus Scrofa Thymus

Viatrexx Bio Incorporated
Human Otc Drug
NDC 63776-027

Aller Balance also known as Choline Chloride, Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Epinephrine, Onion, Ammonium Carbonate, Apis Mellifera, Arsenic Trioxide, Histamine, Interferon Gamma-1a, Interleukin-12 Human, Manganese Gluconate, Luffa Operculata Fruit, Sus Scrofa Lung, Beef Lung, Sus Scrofa Nasal Mucosa, Bos Taurus Nasal Mucosa, Sodium Chloride, Bos Taurus Peyers Patch, Sus Scrofa Peyers Patch, Schoenocaulon Officinale Seed, Serotonin, Bos Taurus Thymus, Sus Scrofa Thymus is a human otc drug labeled by 'Viatrexx Bio Incorporated'. National Drug Code (NDC) number for Aller Balance is 63776-027. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Aller Balance drug includes Ammonium Carbonate - 200 [kp_C]/mL Apis Mellifera - 200 [kp_C]/mL Arsenic Trioxide - 200 [kp_C]/mL Beef Lung - 200 [kp_C]/mL Bos Taurus Adrenal Gland - 200 [kp_C]/mL Bos Taurus Nasal Mucosa - 200 [kp_C]/mL Bos Taurus Peyer's Patch - 30 [kp_C]/mL Bos Taurus Thymus - 200 [kp_C]/mL Choline Chloride - 200 [kp_C]/mL Epinephrine - 30 [kp_C]/mL and more. The currest status of Aller Balance drug is Active.

Drug Information:

Drug NDC:	63776-027
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:	Aller Balance
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:	Choline Chloride, Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Epinephrine, Onion, Ammonium Carbonate, Apis Mellifera, Arsenic Trioxide, Histamine, Interferon Gamma-1a, Interleukin-12 Human, Manganese Gluconate, Luffa Operculata Fruit, Sus Scrofa Lung, Beef Lung, Sus Scrofa Nasal Mucosa, Bos Taurus Nasal Mucosa, Sodium Chloride, Bos Taurus Peyers Patch, Sus Scrofa Peyers Patch, Schoenocaulon Officinale Seed, Serotonin, Bos Taurus Thymus, Sus Scrofa Thymus
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Viatrexx Bio Incorporated
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Spray
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:	AMMONIUM CARBONATE - 200 [kp_C]/mL APIS MELLIFERA - 200 [kp_C]/mL ARSENIC TRIOXIDE - 200 [kp_C]/mL BEEF LUNG - 200 [kp_C]/mL BOS TAURUS ADRENAL GLAND - 200 [kp_C]/mL BOS TAURUS NASAL MUCOSA - 200 [kp_C]/mL BOS TAURUS PEYER'S PATCH - 30 [kp_C]/mL BOS TAURUS THYMUS - 200 [kp_C]/mL CHOLINE CHLORIDE - 200 [kp_C]/mL EPINEPHRINE - 30 [kp_C]/mL Load more... HISTAMINE - 200 [kp_C]/mL INTERFERON GAMMA-1A - 200 [kp_C]/mL INTERLEUKIN-12 HUMAN - 200 [kp_C]/mL LUFFA OPERCULATA FRUIT - 30 [kp_C]/mL MANGANESE GLUCONATE - 4 [hp_X]/mL ONION - 200 [kp_C]/mL SCHOENOCAULON OFFICINALE SEED - 200 [kp_C]/mL SEROTONIN - 200 [kp_C]/mL SODIUM CHLORIDE - 200 [kp_C]/mL SUS SCROFA ADRENAL GLAND - 200 [kp_C]/mL SUS SCROFA LUNG - 200 [kp_C]/mL SUS SCROFA NASAL MUCOSA - 200 [kp_C]/mL SUS SCROFA PEYER'S PATCH - 30 [kp_C]/mL SUS SCROFA THYMUS - 200 [kp_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:	24 Jul, 2012
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	22 Jun, 2026
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:	31 Dec, 2023
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:	VIATREXX BIO INCORPORATED
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.
UPC:	0063776027152
UPC stands for Universal Product Code.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 N0000000209 N0000000245 N0000175552 N0000175555 N0000175570 M0003647 N0000185371 M0006342 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	NJ5VT0FKLJ 7S82P3R43Z S7V92P67HO 2I1RTO1MBR M2776SWB29 343455G79K XB9AHC8DW1 8XEJ88V2T8 45I14D8O27 YKH834O4BH Load more... 820484N8I3 VC9M78242P 7B590791ER C4MO6809HU 9YY2F980SV 492225Q21H 6NAF1689IO 333DO1RDJY 451W47IQ8X 398IYQ16YV 7GL3G1COB3 ID3Z1X61WY 308LM01C72 7B69B0BD62
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 MOA:	Adrenergic alpha-Agonists [MoA] Adrenergic beta-Agonists [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC] alpha-Adrenergic Agonist [EPC] beta-Adrenergic Agonist [EPC] Catecholamine [EPC] Non-Standardized Food 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] Catecholamines [CS] Dietary Proteins [CS] Vegetable Proteins [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:	Adrenergic alpha-Agonists [MoA] Adrenergic beta-Agonists [MoA] Allergens [CS] Bee Venoms [CS] Catecholamine [EPC] Catecholamines [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Magnetic Resonance Contrast Activity [MoA] Non-Standardized Food Allergenic Extract [EPC] Paramagnetic Contrast Agent [EPC] Standardized Insect Venom Allergenic Extract [EPC] Vegetable Proteins [CS] alpha-Adrenergic Agonist [EPC] beta-Adrenergic Agonist [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
63776-027-15	1 BOTTLE, SPRAY in 1 BOX (63776-027-15) / 50 mL in 1 BOTTLE, SPRAY	24 Jul, 2012	N/A	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

Aller Balance

Choline Chloride & more..

Spray
VIATREXX BIO INCORPORATED
NDC: 63776-027

Purpose:

Purpose: choline chloride mental clarity adrenal gland adrenal support adrenalinum adrenal support allium cepa drainage ammonium carbonicum drainage apis inflammation arsenicum album constitution support histamine ig support interferon gamma immune support interleukin-12 immune support manganese gluconate oligo support luffa operculata reactional support lungs respiratory support mucosa respiratory support natrium muraticum constitutional peyer's patch immune support sabadila symptom relief serotonin neurological support thymus immune support

Product Elements:

Aller balance choline chloride, bos taurus adrenal gland, sus scrofa adrenal gland, epinephrine, onion, ammonium carbonate, apis mellifera, arsenic trioxide, histamine, interferon gamma-1a, interleukin-12 human, manganese gluconate, luffa operculata fruit, sus scrofa lung, beef lung, sus scrofa nasal mucosa, bos taurus nasal mucosa, sodium chloride, bos taurus peyers patch, sus scrofa peyers patch, schoenocaulon officinale seed, serotonin, bos taurus thymus, sus scrofa thymus alcohol water choline chloride choline bos taurus adrenal gland bos taurus adrenal gland sus scrofa adrenal gland sus scrofa adrenal gland epinephrine epinephrine onion onion ammonium carbonate ammonium cation apis mellifera apis mellifera arsenic trioxide arsenic cation (3+) histamine histamine interferon gamma-1a interferon gamma-1a interleukin-12 human interleukin-12 human manganese gluconate manganese cation (2+) luffa operculata fruit luffa operculata fruit sus scrofa lung sus scrofa lung beef lung beef lung sus scrofa nasal mucosa sus scrofa nasal mucosa bos taurus nasal mucosa bos taurus nasal mucosa sodium chloride chloride ion bos taurus peyer's patch bos taurus peyer's patch sus scrofa peyer's patch sus scrofa peyer's patch schoenocaulon officinale seed schoenocaulon officinale seed serotonin serotonin bos taurus thymus bos taurus thymus sus scrofa thymus sus scrofa thymus

Indications and Usage:

Uses to assist with balancing the terrain associated with sensitivities

Warnings:

Warnings stop use and ask a health care practitioner if symptoms persist for more than five days or worsen. if pregnant or breastfeeding, ask a health care practitioner before use.

Dosage and Administration:

Dosage 1-5 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Package Label Principal Display Panel:

Principal display panel item: vpc0019 ndc 63776-027-15 homeopathic remedy aller balance â¢ to assist with balancing the terrain associated with sensitivities oral spray 50ml 1.7 oz viatrexx â¢ bio incorporated manufactured by viatrexx www.viatrexx.com newark, de 19713 aller balance 50 ml 1.7 oz viatrexx â¢ bio incorporated item: vpc0019 ndc: 63776-027-15 indications: to assit with balancing the terrain associated with sensitivities. directions: 1-5 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner. mfg. for viatrexx bio incorporated. www.viatrexx.com newark, de 19713 carton label

Further Questions:

Questions info@viatrexx.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.