NDC 63083-9420 Thyroid Nosode Combination 9420
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-9420?
What are the uses for Thyroid Nosode Combination 9420?
Which are Thyroid Nosode Combination 9420 UNII Codes?
The UNII codes for the active ingredients in this product are:
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- OXOGLURIC ACID (UNII: 8ID597Z82X)
- OXOGLURIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- MALIC ACID (UNII: 817L1N4CKP)
- MALIC ACID (UNII: 817L1N4CKP) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B)
- PULSATILLA MONTANA WHOLE (UNII: 24K790T39B) (Active Moiety)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
Which are Thyroid Nosode Combination 9420 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".