NDC 50181-0023 Endopure Estro

Estriol, Estradiol, Folliculinum, Belladonna, Chelidonium Majus, Hydrocortisone, Glandula Suprarenalis Suis, Hypothalamus Suis, Oophorinum Suis, Pineal Suis, Pituitary Suis, Sanguinaria Canadensis, Lilium Tigrinum, Pulsatilla, Sepia, Sulphur

NDC Product Code 50181-0023

NDC Code: 50181-0023

Proprietary Name: Endopure Estro 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: Estriol, Estradiol, Folliculinum, Belladonna, Chelidonium Majus, Hydrocortisone, Glandula Suprarenalis Suis, Hypothalamus Suis, Oophorinum Suis, Pineal Suis, Pituitary Suis, Sanguinaria Canadensis, Lilium Tigrinum, Pulsatilla, 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
    • 50181-0023 - Endopure Estro

NDC 50181-0023-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Endopure Estro with NDC 50181-0023 is a a human over the counter drug product labeled by The Wellness Center For Research And Education. The generic name of Endopure Estro is estriol, estradiol, folliculinum, belladonna, chelidonium majus, hydrocortisone, glandula suprarenalis suis, hypothalamus suis, oophorinum suis, pineal suis, pituitary suis, sanguinaria canadensis, lilium tigrinum, pulsatilla, sepia, sulphur. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center For Research And Education

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 Estro 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.

  • ESTRIOL 6 [hp_X]/mL
  • ESTRADIOL 6 [hp_X]/mL
  • ESTRONE 6 [hp_X]/mL
  • ATROPA BELLADONNA WHOLE 6 [hp_C]/mL
  • CHELIDONIUM MAJUS 6 [hp_C]/mL
  • HYDROCORTISONE 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
  • SUS SCROFA PINEAL GLAND 6 [hp_C]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_C]/mL
  • SANGUINARIA CANADENSIS ROOT 6 [hp_C]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_C]/mL
  • PULSATILLA VULGARIS 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
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: 04-04-2013 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: 12-31-2019 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 Estro Product Label Images

Endopure Estro 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:

Estriol 6X, Estradiol 6X, Folliculinum 6X, Belladonna 6C, Chelidonium Majus 6C, Cortisol (Hydrocortisone) 6C, Glandula Suprarenalis Suis 6C, Hypothalamus (Suis) 6C, Oophorinum (Suis) 6C, Pineal (Suis) 6C, Pituitary (Suis) 6C, Sanguinaria Canadensis 6C, Lilium Tigrinum 12C, Pulsatilla 12C, Sepia 12C, Sulphur 12C

Indications:

For the temporary relief of hot flashes, climacteric complaints, ovarian complaints and pain, liver complaints, depression, menses scanty; stopped or late, irritable, uterine and vaginal complaints.

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 around neck is broken or missing.  Store in a cool, dry place.

Directions For Use:

5 drops orally 2 to 3 times daily between meals.  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 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, Ethanol 25%

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.

Indications And Usage:

For the temporary relief of hot flashes, climacteric complaints, ovarian complaints and pain, liver complaints, depression, menses scanty; stopped or late, irritable, uterine and vaginal complaints.

Questions:

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

Package Label Display:

NDC 50181-0023-1EndoPureby Theresa Dale, Ph.D, CCNHomeopathicESTROHORMONE REJUVENATION SYSTEM 1 FL OZ (30 ml)

* Please review the disclaimer below.

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