NDC 63083-3021 Thyroid Liquescence 3021
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-3021?
What are the uses for Thyroid Liquescence 3021?
Which are Thyroid Liquescence 3021 UNII Codes?
The UNII codes for the active ingredients in this product are:
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- SKIM MILK (UNII: 6A001Y4M5A)
- SKIM MILK (UNII: 6A001Y4M5A) (Active Moiety)
- MOLYBDENUM (UNII: 81AH48963U)
- MOLYBDENUM (UNII: 81AH48963U) (Active Moiety)
- ENTEROBIUS VERMICULARIS (UNII: W1D68QW48M)
- ENTEROBIUS VERMICULARIS (UNII: W1D68QW48M) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3)
- CALCIUM HEXAFLUOROSILICATE (UNII: 2NVP93XVQ3) (Active Moiety)
- REDUCTIC ACID (UNII: 46L13F32TC)
- REDUCTIC ACID (UNII: 46L13F32TC) (Active Moiety)
Which are Thyroid Liquescence 3021 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
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[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".