NDC 57955-0033 Tremorplex
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-0033?
What are the uses for Tremorplex?
Which are Tremorplex UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037)
- AMANITA MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO) (Active Moiety)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3)
- HYOSCYAMUS NIGER (UNII: 4WRK2153H3) (Active Moiety)
- MANGANESE ACETATE TETRAHYDRATE (UNII: 9TO51D176N)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
Which are Tremorplex 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)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".