NDC 63776-033 Ans/cns

Choline Chloride, Epinephrine, .gamma.-aminobutyric Acid, Histamine, Goldenseal, Norepinephrine, Taraxacum Palustre Root, Tyramine

NDC Product Code 63776-033

NDC CODE: 63776-033

Proprietary Name: Ans/cns 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: Choline Chloride, Epinephrine, .gamma.-aminobutyric Acid, Histamine, Goldenseal, Norepinephrine, Taraxacum Palustre Root, Tyramine 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

  • 63776 - Viatrexx Bio Incorporated

NDC 63776-033-15

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Ans/cns with NDC 63776-033 is a a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Ans/cns is choline chloride, epinephrine, .gamma.-aminobutyric acid, histamine, goldenseal, norepinephrine, taraxacum palustre root, tyramine. The product's dosage form is spray and is administered via oral form.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Ans/cns 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.

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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: Viatrexx Bio Incorporated
Labeler Code: 63776
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: 07-24-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Ans/cns 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

Choline Chloride 6X 200K, Adrenalin 6X 200K, GABA 6X 200K, Histamine 6X 200K, Hydrastis 3X, Norepinephrine 6X 200K, Taraxacum 3X 30K, Tyramine 6X 200K


Choline ChlorideMental clarityAdrenalinAdrenal supportGABAMental clarityHistamineIg supportHydrastisDrainageNorepinephrineAdrenal supportTaraxacumDrainageTyramineNeurological support


For the support & balancing of the Anatomic & Central nervous systems


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.


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

Other Ingredients

Alcohol and Water

Other Information

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


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* Please review the disclaimer below.