NDC 63776-027 Aller Balance
Choline Chloride, Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Epinephrine, Oni...

Product Information

What is NDC 63776-027?

The NDC code 63776-027 is assigned by the FDA to the product Aller Balance which is a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Aller Balance is 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. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 63776-027-15 1 bottle, spray in 1 box / 50 ml in 1 bottle, spray. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code63776-027
Proprietary Name 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.		Aller Balance
Non-Proprietary Name 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.		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
Product Type 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.		Human Otc Drug
Dosage FormSpray - A liquid minutely divided as by a jet of air or steam.
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.		Viatrexx Bio Incorporated
Labeler Code63776
Marketing Category 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.		UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		07-24-2012
Listing Expiration Date What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.		12-31-2023
Exclude Flag 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I". 		N
NDC Code Structure

What are the uses for Aller Balance?


Product Packages

NDC Code 63776-027-15

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 50 mL in 1 BOTTLE, SPRAY

Product Details

What are Aller Balance Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Aller Balance Active Ingredients UNII Codes

Aller Balance Inactive Ingredients UNII Codes

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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Aller Balance Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredients



Choline chloride (15X, 200K), Histamine (15X, 200K), Serotonin (15X, 200K), Adrenal gland (200K), Allium Cepa (200K), Ammonium carbonicum (200K), Apis (200K), Arsenicum album (200K), Lungs (200K), Mucosa (200K), Natrium Mur (200K), Sabadila (200K), Thymus (200K), Adrenalinum (30K), Luffa operculata (30K), Peyer's Patches (30K), Interferon gamma (9X, 200K), Interleukin-12 (10X, 200K), Manganese gluconate (4X)


Purpose:



Choline chlorideMental clarity
Adrenal glandAdrenal support
AdrenalinumAdrenal support
Allium cepaDrainage
Ammonium carbonicumDrainage
ApisInflammation
Arsenicum albumConstitution support
HistamineIG support
Interferon gammaImmune support
Interleukin-12Immune support
Manganese gluconateOligo support
Luffa operculataReactional support
LungsRespiratory support
MucosaRespiratory support
Natrium MuraticumConstitutional
Peyer's PatchImmune support
Sabadilasymptom relief
SerotoninNeurological support
ThymusImmune support

Uses



To assist with balancing the terrain associated with sensitivities


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



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


Other Ingredients



20% Alcohol and 80% Water.


Other Information



Normal storage use.

Do not use if tamper-evident seal is broken or removed.


Questions



[email protected]


Principal Display Panel



ITEM: VPC0019

NDC 63776-027-15

Homeopathic remedy

Aller Balance

• To assist with balancing the terrain associated with sensitivities

Oral spray
50ml 1.7 oz

Viatrexx™ Bio Incorporated

Manufactured by Viatrexx
www.viatrexx.com
Newark, DE 19713

carton - allerbalancecarton

carton - allerbalancecarton

Aller Balance

50 ml
1.7 oz

Viatrexx™ 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


* Please review the disclaimer below.