Female

Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Cholesterol, Sus Scrofa Corpus Luteum, Esterified Estrogen, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Melatonin, Bos Taurus Ovary, Sus Scrofa Ovary, Bos Taurus Pancreas, Sus Scrofa Pancreas, Bos Taurus Pineal Gland, Sus Scrofa Pineal Gland, Bos Taurus Pituitary Gland, Sus Scrofa Pituitary Gland, Progesterone, Sus Scrofa Thalamus, Bos Taurus Thymus, Sus Scrofa Thymus, Thyroid Bovine, Thyroid Porcine


Viatrexx Bio Incorporated
Human Otc Drug
NDC 63776-171
Female also known as Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Cholesterol, Sus Scrofa Corpus Luteum, Esterified Estrogen, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Melatonin, Bos Taurus Ovary, Sus Scrofa Ovary, Bos Taurus Pancreas, Sus Scrofa Pancreas, Bos Taurus Pineal Gland, Sus Scrofa Pineal Gland, Bos Taurus Pituitary Gland, Sus Scrofa Pituitary Gland, Progesterone, Sus Scrofa Thalamus, Bos Taurus Thymus, Sus Scrofa Thymus, Thyroid Bovine, Thyroid Porcine is a human otc drug labeled by 'Viatrexx Bio Incorporated'. National Drug Code (NDC) number for Female is 63776-171. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Female drug includes Bos Taurus Adrenal Gland - 200 [kp_C]/mL Bos Taurus Hypothalamus - 200 [kp_C]/mL Bos Taurus Ovary - 200 [kp_C]/mL Bos Taurus Pancreas - 200 [kp_C]/mL Bos Taurus Pineal Gland - 200 [kp_C]/mL Bos Taurus Pituitary Gland - 200 [kp_C]/mL Bos Taurus Thymus - 200 [kp_C]/mL Cholesterol - 200 [kp_C]/mL Estrogens, Esterified - 200 [kp_C]/mL Melatonin - 200 [kp_C]/mL and more. The currest status of Female drug is Active.

Drug Information:

Drug NDC: 63776-171
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: Female
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: Bos Taurus Adrenal Gland, Sus Scrofa Adrenal Gland, Cholesterol, Sus Scrofa Corpus Luteum, Esterified Estrogen, Bos Taurus Hypothalamus, Sus Scrofa Hypothalamus, Melatonin, Bos Taurus Ovary, Sus Scrofa Ovary, Bos Taurus Pancreas, Sus Scrofa Pancreas, Bos Taurus Pineal Gland, Sus Scrofa Pineal Gland, Bos Taurus Pituitary Gland, Sus Scrofa Pituitary Gland, Progesterone, Sus Scrofa Thalamus, Bos Taurus Thymus, Sus Scrofa Thymus, Thyroid Bovine, Thyroid Porcine
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:BOS TAURUS ADRENAL GLAND - 200 [kp_C]/mL
BOS TAURUS HYPOTHALAMUS - 200 [kp_C]/mL
BOS TAURUS OVARY - 200 [kp_C]/mL
BOS TAURUS PANCREAS - 200 [kp_C]/mL
BOS TAURUS PINEAL GLAND - 200 [kp_C]/mL
BOS TAURUS PITUITARY GLAND - 200 [kp_C]/mL
BOS TAURUS THYMUS - 200 [kp_C]/mL
CHOLESTEROL - 200 [kp_C]/mL
ESTROGENS, ESTERIFIED - 200 [kp_C]/mL
MELATONIN - 200 [kp_C]/mL
PROGESTERONE - 200 [kp_C]/mL
SUS SCROFA ADRENAL GLAND - 200 [kp_C]/mL
SUS SCROFA CORPUS LUTEUM - 200 [kp_C]/mL
SUS SCROFA HYPOTHALAMUS - 200 [kp_C]/mL
SUS SCROFA OVARY - 200 [kp_C]/mL
SUS SCROFA PANCREAS - 200 [kp_C]/mL
SUS SCROFA PINEAL GLAND - 200 [kp_C]/mL
SUS SCROFA PITUITARY GLAND - 200 [kp_C]/mL
SUS SCROFA THALAMUS - 200 [kp_C]/mL
SUS SCROFA THYMUS - 200 [kp_C]/mL
THYROID, BOVINE - 200 [kp_C]/mL
THYROID, PORCINE - 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: 10 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:0063776171152
UPC stands for Universal Product Code.
NUI:M0017672
N0000175601
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:M2776SWB29
S6G2NLH4Y7
66LZN1C747
1M529TNT1D
Z7RM5NBH36
7JM57I419K
8XEJ88V2T8
97C5T2UQ7J
3ASP8Q3768
JL5DK93RCL
4G7DS2Q64Y
398IYQ16YV
94X749MHSP
N6R0856Z79
S7YTV04R8O
9Y3J3362RY
050QZ2EDK7
L0PFEMQ1DT
3D6Q7UV74J
7B69B0BD62
MN18OTN73W
6RV024OAUQ
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:Progesterone [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 CS:Progesterone [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:Progesterone [CS]
Progesterone [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63776-171-151 BOTTLE, SPRAY in 1 BOX (63776-171-15) / 50 mL in 1 BOTTLE, SPRAY24 Jul, 2012N/ANo
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.

Purpose:

Purpose adrenal gland adrenal support cholesterinum drainage corpus luteum regeneration estrogen hormonal support hypothalamus regeneration melatonin neurological support ovary regeneration pancreas regeneration pineal gland regeneration pituitary regeneration progesterone hormonal support thalamus gland regeneration thymus gland regeneration thyroid gland regeneration

Product Elements:

Female bos taurus adrenal gland, sus scrofa adrenal gland, cholesterol, sus scrofa corpus luteum, esterified estrogen, bos taurus hypothalamus, sus scrofa hypothalamus, melatonin, bos taurus ovary, sus scrofa ovary, bos taurus pancreas, sus scrofa pancreas, bos taurus pineal gland, sus scrofa pineal gland, bos taurus pituitary gland, sus scrofa pituitary gland, progesterone, sus scrofa thalamus, bos taurus thymus, sus scrofa thymus, thyroid bovine, thyroid porcine alcohol water bos taurus adrenal gland bos taurus adrenal gland sus scrofa adrenal gland sus scrofa adrenal gland cholesterol cholesterol sus scrofa corpus luteum sus scrofa corpus luteum estrogens, esterified estrogens, esterified bos taurus hypothalamus bos taurus hypothalamus sus scrofa hypothalamus sus scrofa hypothalamus melatonin melatonin bos taurus ovary bos taurus ovary sus scrofa ovary sus scrofa ovary bos taurus pancreas bos taurus pancreas sus scrofa pancreas sus scrofa pancreas bos taurus pineal gland bos taurus pineal gland sus scrofa pineal gland sus scrofa pineal gland bos taurus pituitary gland bos taurus pituitary gland sus scrofa pituitary gland sus scrofa pituitary gland progesterone progesterone sus scrofa thalamus sus scrofa thalamus bos taurus thymus bos taurus thymus sus scrofa thymus sus scrofa thymus thyroid, bovine thyroid, bovine thyroid, porcine thyroid, porcine

Indications and Usage:

Uses to help support the structure & function of the female endocrine system

Warnings:

Warnings stop use and ask a health care practitioner if symptoms persist for more than 5 days or worsen. if pregnant or breastfeeding, ask a health care practitioner before use.

Dosage and Administration:

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

Package Label Principal Display Panel:

Principal display panel item: vpc0187 ndc 63776-171-15 homeopathic remedy female + • to help support the structure & function of the female endocrine system oral spray 50ml 1.7 oz viatrexx ™ bio incorporated manufactured by viatrexx www.viatrexx.com newark, de 19713 female + 50 ml 1.7 oz viatrexx ™ bio incorporated item: vpc0187 ndc: 63776-171-15 indications: to help support the structure & function of the female endocrine system 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 female + box ingredients

Further Questions:

Questions info@viatrexx.com


Comments/ Reviews:

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