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  4. NDC Product Code: 50181-0074 Endopure Testos For Women

NDC 50181-0074 Endopure Testos For Women

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50181-0074?
  4. Endopure Testos For Women Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50181-0074
Proprietary Name:
Endopure Testos For Women
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Wellness Center For Research And Education, Inc.
Labeler Code:
50181
Product Label ID:
04702cd6-ce49-43d2-bc5e-7a9e19815fe7
Start Marketing Date: [9]
04-19-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50181-0074-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 50181-0074?

The NDC code 50181-0074 is assigned by the FDA to the product Endopure Testos For Women which is product labeled by The Wellness Center For Research And Education, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50181-0074-1 30 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Endopure Testos For Women?

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.

Which are Endopure Testos For Women UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Endopure Testos For Women 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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".