NDC 52389-171 Psoriasin Therapeutic Shampoo And Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52389 - Alva-amco Pharmacal Companies, Inc.
- 52389-171 - Psoriasin
Product Packages
NDC Code 52389-171-06
Package Description: 185 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52389-171?
What are the uses for Psoriasin Therapeutic Shampoo And Body Wash?
Which are Psoriasin Therapeutic Shampoo And Body Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Psoriasin Therapeutic Shampoo And Body Wash 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:
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- PANTHENOL (UNII: WV9CM0O67Z)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
What is the NDC to RxNorm Crosswalk for Psoriasin Therapeutic Shampoo And Body Wash?
- RxCUI: 1046277 - salicylic acid 3 % Medicated Liquid Soap
- RxCUI: 1046277 - salicylic acid 30 MG/ML Medicated Liquid Soap
- RxCUI: 1046281 - Psoriasin Therapeutic Shampoo & Body Wash 3 % Medicated Liquid Soap
- RxCUI: 1046281 - salicylic acid 30 MG/ML Medicated Liquid Soap [Psoriasin Wash]
- RxCUI: 1046281 - Psoriasin Wash 30 MG/ML Medicated Liquid Soap
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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".