NDC 50181-0031 Mercury Plus Detox
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50181-0031?
What are the uses for Mercury Plus Detox?
Which are Mercury Plus Detox UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- PORK BRAIN (UNII: 466251J72G)
- PORK BRAIN (UNII: 466251J72G) (Active Moiety)
- SUS SCROFA SPINAL CORD (UNII: AVM99FC8AI)
- SUS SCROFA SPINAL CORD (UNII: AVM99FC8AI) (Active Moiety)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
- THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
- UNITHIOL (UNII: 690VN2L7TK)
- 2,3-DIMERCAPTO-1-PROPANESULFONIC ACID (UNII: 086L82361J) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- MERCURY (UNII: FXS1BY2PGL)
- MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
- THIMEROSAL (UNII: 2225PI3MOV)
- ETHYLMERCURITHIOSALICYLIC ACID (UNII: 4071N4J64W) (Active Moiety)
Which are Mercury Plus Detox 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".