NDC 0256-0210 Thyroshield
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0256 - Fleming & Company, Pharmaceuticals
- 0256-0210 - Thyroshield
Product Characteristics
Product Packages
NDC Code 0256-0210-01
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 0256-0210?
What are the uses for Thyroshield?
Which are Thyroshield UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE I-125 (UNII: V1UJ6I93CL) (Active Moiety)
Which are Thyroshield 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SUCROSE (UNII: C151H8M554)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Thyroshield?
- RxCUI: 242429 - potassium iodide 325 MG in 5 mL Oral Solution
- RxCUI: 242429 - potassium iodide 65 MG/ML Oral Solution
- RxCUI: 242429 - K+ Iodide 65 MG/ML Oral Solution
- RxCUI: 242429 - Pot Iodide 65 MG/ML Oral Solution
- RxCUI: 242429 - potassium iodide 325 MG per 5 ML Oral Solution
* 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".