NDC 50169-0001 Type 4 Noise Regular
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50169 - T Gone Remedies
- 50169-0001 - Type 4 Noise Regular
Product Characteristics
Product Packages
NDC Code 50169-0001-1
Package Description: 15000 mg in 1 BOTTLE
Product Details
What is NDC 50169-0001?
What are the uses for Type 4 Noise Regular?
Which are Type 4 Noise Regular UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- QUININE SULFATE (UNII: KF7Z0E0Q2B)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- ALLYLTHIOUREA (UNII: 706IDJ14B7)
- ALLYLTHIOUREA (UNII: 706IDJ14B7) (Active Moiety)
Which are Type 4 Noise Regular 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
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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".