NDC 50181-0066 Endopure Pro

L-arginine, Hypophysis Suis, Pineal (suis), Progesterone, Belladonna, Chelidonium Majus, Dioscorea Villosa, Folliculinum, Glandula Suprarenalis Suis, Hypothalamus Suis, Oophorinum (suis), Lilium Tigrinum, Pulsatilla (vulgaris), Sepia, Sulphur

NDC Product Code 50181-0066

NDC Code: 50181-0066

Proprietary Name: Endopure Pro 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: L-arginine, Hypophysis Suis, Pineal (suis), Progesterone, Belladonna, Chelidonium Majus, Dioscorea Villosa, Folliculinum, Glandula Suprarenalis Suis, Hypothalamus Suis, Oophorinum (suis), Lilium Tigrinum, Pulsatilla (vulgaris), Sepia, Sulphur 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.
    • 50181-0066 - Endopure Pro

NDC 50181-0066-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Endopure Pro with NDC 50181-0066 is a a human over the counter drug product labeled by The Wellness Center For Research And Education, Inc.. The generic name of Endopure Pro is l-arginine, hypophysis suis, pineal (suis), progesterone, belladonna, chelidonium majus, dioscorea villosa, folliculinum, glandula suprarenalis suis, hypothalamus suis, oophorinum (suis), lilium tigrinum, pulsatilla (vulgaris), sepia, sulphur. 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.

Endopure Pro 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.

  • ARGININE 6 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 6 [hp_X]/mL
  • PROGESTERONE 6 [hp_X]/mL
  • ATROPA BELLADONNA 6 [hp_C]/mL
  • CHELIDONIUM MAJUS 6 [hp_C]/mL
  • DIOSCOREA VILLOSA TUBER 6 [hp_C]/mL
  • ESTRONE 6 [hp_C]/mL
  • SUS SCROFA ADRENAL GLAND 6 [hp_C]/mL
  • SUS SCROFA HYPOTHALAMUS 6 [hp_C]/mL
  • SUS SCROFA OVARY 6 [hp_C]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_C]/mL
  • ANEMONE PULSATILLA 12 [hp_C]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_C]/mL
  • SULFUR 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: 04-11-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Endopure Pro Product Label Images

Endopure Pro 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:

L-Arginine 6X, Hypophysis Suis 6X, Pineal (Suis) 6X, Progesterone 6X, Belladonna 6C, Chelidonium Majus 6C, Dioscorea Villosa 6C, Folliculinum 6C, Glandula Suprarenalis Suis 6C, Hypothalamus Suis 6C, Oophorinum (Suis) 6C, Lilium Tigrinum 12C, Pulsatilla (Vulgaris) 12C, Sepia 12C, Sulphur 12C.

Homeopathic Indications:

For the temporary relief of hot flashes, stopped, scanty or late menses, liver and sleep complaints, vaginal and uterine irritability.

For the temporary relief of hot flashes, stopped, scanty or late menses, liver and sleep complaints, vaginal and uterine irritability.

Warnings:

If pregnant or breast-feeding, 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 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. Use Day 10 through Day 21 of the normal menstrual cycle, even if menses has ceased. If cycle dates are unknown, day 1 is the first day of the calendar month. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Manufactured forThe Wellness Center for Researchand Education, Inc.1237 S. Victoria Ave., Suite 169Oxnard, CA 93035www.wellnesscenter.net

Package Label Display:

NDC 50181-0066-1EndoPureby Theresa Dale, Ph.D, CCNHomeopathicPROHORMONE REJUVENATION SYSTEM1 FL. OZ. (30 ml)

* Please review the disclaimer below.

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