NDC 57520-0712 Loma Lux Psoriasis
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57520-0712?
What are the uses for Loma Lux Psoriasis?
Which are Loma Lux Psoriasis UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM BROMIDE (UNII: LC1V549NOM)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68)
- NICKEL (UNII: 7OV03QG267) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- ZINC BROMIDE (UNII: OO7ZBU9703)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Loma Lux Psoriasis 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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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".