NDC 50845-0039 Extreme Thyro Pro

NDC Product Code 50845-0039

NDC 50845-0039-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Extreme Thyro Pro with NDC 50845-0039 is a product labeled by Liddell Laboratories. The generic name of Extreme Thyro Pro is . The product's dosage form is and is administered via form.

Labeler Name: Liddell Laboratories

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)

Product Labeler Information

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

Labeler Name: Liddell Laboratories
Labeler Code: 50845
Start Marketing Date: 08-20-2010 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Extreme Thyro Pro Product Label Images

Extreme Thyro 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

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Amino acids 6X, Apis mellifica 3X, Arnica montana 3X, Fucus vesiculosus 3X, Gambogia 3X, Hepar suis 6X, Phosphoricum acidum 3X, Pituitary suis 24X, Thuja occidentalis 30C, Thyroidinum 30C.

Otc - Purpose

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

Warnings

WARNINGS:  If symptoms persist, consult a physician.  If pregnant or breast-feeding, or if you have a pre-existing medical condition, consult a physician prior to use.DO NOT USE IF TAMPER EVIDENT SEAL AROUND NECK OF BOTTLE IS BROKEN OR MISSING.

Dosage & Administration

DIRECTIONS:  Adults only, spray twice under the tongue, three times a day.

Inactive Ingredient

INACTIVE INGREDIENTS:  Organic alcohol 30% v/v, Purified water.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN:  In case of overdose, get medical help or call a Poison Control Center right away.

Indications & Usage

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

Otc - Questions

Dist. by:Team SprayFlex, LLCHenderson, NV 89052866-311-FLEX  www.SprayFlex.com

* Please review the disclaimer below.