NDC 50544-304 Af Foam Sensitive Acne Pore Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50544 - University Medical Pharmaceuticals Corp
- 50544-304 - Af Foam Sensitive Acne Pore Cleanser
Product Packages
NDC Code 50544-304-40
Package Description: 85 g in 1 CAN
Product Details
What is NDC 50544-304?
What are the uses for Af Foam Sensitive Acne Pore Cleanser?
Which are Af Foam Sensitive Acne Pore Cleanser 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 Af Foam Sensitive Acne Pore Cleanser 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:
- OAT (UNII: Z6J799EAJK)
- LEVOMENOL (UNII: 24WE03BX2T)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- WATER (UNII: 059QF0KO0R)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- GINGER (UNII: C5529G5JPQ)
What is the NDC to RxNorm Crosswalk for Af Foam Sensitive Acne Pore Cleanser?
- RxCUI: 1234456 - salicylic acid 1.5 % Medicated Liquid Soap
- RxCUI: 1234456 - salicylic acid 15 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".