NDC 50845-0039 Extreme Thyro Pro

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50845-0039
Proprietary Name:
Extreme Thyro Pro
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Liddell Laboratories
Labeler Code:
50845
Start Marketing Date: [9]
08-20-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50845-0039-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 50845-0039?

The NDC code 50845-0039 is assigned by the FDA to the product Extreme Thyro Pro which is product labeled by Liddell Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50845-0039-1 30 ml in 1 bottle, spray . 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 Extreme Thyro Pro?

USES:  Provides scientifically proven, multi-angular support for relief from many issues experienced by those who want to lose weight and cut bodyfat.  Benefits may include:  *supports thyroid function  *decreased bodyfat  *enhanced metabolism  *increased muscle tone  *more energy  *reduced food and carbohydrate cravings  *improved digestion and protein synthesis  *reduced excess fluid retention

Which are Extreme Thyro Pro UNII Codes?

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

Which are Extreme Thyro Pro 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:

* Please review the disclaimer below.

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".