NDC 63776-320 Male Plus
Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Aldosterone, Androsterone, Adenosi...

Product Information

What is NDC 63776-320?

The NDC code 63776-320 is assigned by the FDA to the product Male Plus which is a human over the counter drug product labeled by Viatrexx Bio Incorporated. The generic name of Male Plus is bos taurus adrenal gland, sus scrofa adrenal gland, aldosterone, androsterone, adenosine cyclic 3, 5-phosphate, cholesterol, prasterone, somatropin, bos taurus hypothalamus, sus scrofa hypothalamus, melatonin, bos taurus pancreas, sus scrofa pancreas, bos taurus pineal gland, sus scrofa pineal gland, bos taurus pituitary gland, sus scrofa pituitary gland, bos taurus prostate gland, sus scrofa prostate, bos taurus testicle, sus scrofa testicle, testosterone, sus scrofa thalamus. 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 63776-320-15 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 Code63776-320
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.
Male Plus
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.
Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Aldosterone, Androsterone, Adenosine Cyclic 3, 5-phosphate, Cholesterol, Prasterone, Somatropin, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Melatonin, Bos Taurus Pancreas, Sus Scrofa Pancreas, Bos Taurus Pineal Gland, Sus Scrofa Pineal Gland, Bos Taurus Pituitary Gland, Sus Scrofa Pituitary Gland, Bos Taurus Prostate Gland, Sus Scrofa Prostate, Bos Taurus Testicle, Sus Scrofa Testicle, Testosterone, Sus Scrofa Thalamus
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
DEA Schedule What is the Drug Enforcement Administration (DEA) CIII Schedule?
The controlled substances in the CIII schedule have an abuse potential and dependence liability less than those in schedules CI and CII, and have an accepted medical use in the United States. Schedule CIII controlled substances include preparations containing limited quantities of certain narcotic drugs, and other nonnarcotic drugs such as: derivatives of barbituric acid, except those that are listed in another schedule, glutethimide (Doriden), methyprylon (Noludar), nalorphine, benzphetamine, chlorphentermine, clortermine, and phendimetrazine.
Schedule III (CIII) Substances
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.
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.
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.
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".
NDC Code Structure

What are the uses for Male Plus?

Product Packages

NDC Code 63776-320-15

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

Product Details

What are Male Plus 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.

Male Plus Active Ingredients UNII Codes

Male Plus 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.

Male Plus 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

Adrenal gland (6X, 200K), Aldosterone (15X, 200K), Androsterone (15X, 200K), cAMP / Adenosinum cyclophosphoricum (6X, 200K), Cholesterinum (6X, 200K), DHEA (6X, 200K), Growth hormone (4C, 200K), Hypothalamus (8X, 200K), Melatonin (4C, 200K), Pancreas (6X, 200K), Pineal (6X, 200K), Pituitary (6X, 200K), Prostate (6X, 200K), Testis (6X, 200K), Testosterone (6X, 200K), Thalamus (6X, 200K), Thymus (6C, 200K), Thyroid gland (200K)


Adrenal glandAdrenal support
AldosteroneHormonal support
AndrosteroneAdrenal support
cAMP / Adenosinum cyclophosphoricumIntra-Cellular support
DHEAAdrenal support
Growth hormoneHormonal support
MelatoninNeurological support
TestosteroneHormonal support
Thyroid glandRegeneration


To help support the structure & function of the male endocrine system


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.

Inactive Ingredients

20% Alcohol and 80% Water

Other Information

Normal storage use.

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


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Principal Display Panel


NDC 63776-320-15

Homeopathic remedy

Male +

• To help support the structure & functin of the male endocrine system

Oral spray
50ml 1.7 oz

Viatrexx™ Bio Incorporated

Manufactured by Viatrexx
Newark, DE 19713

Male +

50 ml
1.7 oz

Viatrexx™ Bio Incorporated

NDC: 63776-320-15

To help support the structure & function of the male endocrine system

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

Mfg. for
Viatrexx Bio Incorporated.
Newark, DE 19713

* Please review the disclaimer below.