NDC 50181-0074 Endopure Testos For Women

Hypothalamus Suis, Rna, Sabal Serrulata, Dna, Glandula Suprarenalis Suis, Hydrocortisone (cortisol), Hypophysis Suis, Testosterone, Chelidonium Majus, Thuja Occidentalis

NDC Product Code 50181-0074

NDC CODE: 50181-0074

Proprietary Name: Endopure Testos For Women 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: Hypothalamus Suis, Rna, Sabal Serrulata, Dna, Glandula Suprarenalis Suis, Hydrocortisone (cortisol), Hypophysis Suis, Testosterone, Chelidonium Majus, Thuja Occidentalis 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

  • 50181 - The Wellness Center For Research And Education, Inc.

NDC 50181-0074-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Endopure Testos For Women with NDC 50181-0074 is a a human over the counter drug product labeled by The Wellness Center For Research And Education, Inc.. The generic name of Endopure Testos For Women is hypothalamus suis, rna, sabal serrulata, dna, glandula suprarenalis suis, hydrocortisone (cortisol), hypophysis suis, testosterone, chelidonium majus, thuja occidentalis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center For Research And Education, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

DEA Schedule: Schedule III (CIII) Substances 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.

Endopure Testos For Women 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.

  • SUS SCROFA HYPOTHALAMUS 6 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE RNA 6 [hp_X]/mL
  • SAW PALMETTO 6 [hp_X]/mL
  • HERRING SPERM DNA 6 [hp_C]/mL
  • SUS SCROFA ADRENAL GLAND 6 [hp_C]/mL
  • HYDROCORTISONE 6 [hp_C]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_C]/mL
  • TESTOSTERONE 6 [hp_C]/mL
  • CHELIDONIUM MAJUS WHOLE 12 [hp_C]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_C]/mL

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.

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

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: The Wellness Center For Research And Education, Inc.
Labeler Code: 50181
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: 04-19-2021 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: 12-31-2022 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.

Endopure Testos For Women Product Label Images

Endopure Testos For Women 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:

Hypothalamus Suis 6X, RNA 6X, Sabal Serrulata 6X, DNA 6C, Glandula Suprarenalis Suis 6C, Hydrocortisone (Cortisol) 6C, Hypophysis Suis 6C, Testosterone 6C, Chelidonium Majus 12C, Thuja Occidentalis 12C.

Indications:

For the temporary relief of the following complaints: liver, hot flashes, and irregular periods.

For the temporary relief of the following complaints: liver, hot flashes, and irregular periods.

Warnings:

If pregnant or breastfeeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal around neck is broken or missing.Store in a cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

5 drops orally 2 to 3 times daily between meals.Female: Administer orally, day 1 through 24 of the monthly menstrual cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first day of the calendar month. Use 5 drops between 7:30 and 8:30 pm and upon waking.Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Organic Ethanol

Questions:

Manufactured forThe Wellness Center forResearch and Education, Inc.1237 S. Victoria Ave., Ste. 169Oxnard, CA 93035www.wellnesscenter.net

Package Label Display:

NDC 50181-0074-1EndoPureby Theresa Dale, Ph.D, CCNHomeopathicTESTOS(For Women)HORMONE REJUVENATION SYSTEM1 FL. OZ. (30 ml)

* Please review the disclaimer below.