NDC 50181-0002 Thyro T3 Rescue
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Research And Education
- 50181-0002 - Thyro T3 Rescue
Product Packages
NDC Code 50181-0002-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0002?
What are the uses for Thyro T3 Rescue?
Which are Thyro T3 Rescue UNII Codes?
The UNII codes for the active ingredients in this product are:
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- BOS TAURUS PARATHYROID GLAND (UNII: SMV71DDI4T)
- BOS TAURUS PARATHYROID GLAND (UNII: SMV71DDI4T) (Active Moiety)
- SELENIUM (UNII: H6241UJ22B)
- SELENIUM (UNII: H6241UJ22B) (Active Moiety)
- THYROID, PORCINE (UNII: 6RV024OAUQ)
- THYROID, PORCINE (UNII: 6RV024OAUQ) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
- LEVOTHYROXINE (UNII: Q51BO43MG4)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
- LIOTHYRONINE (UNII: 06LU7C9H1V)
- LIOTHYRONINE (UNII: 06LU7C9H1V) (Active Moiety)
Which are Thyro T3 Rescue 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".