NDC 73740-4040 Biosilk
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73740 - Farouk Systems, Inc.
- 73740-4040 - Biosilk
Product Packages
NDC Code 73740-4040-1
Package Description: 340 g in 1 BOTTLE, PUMP
NDC Code 73740-4040-5
Package Description: 739 g in 1 BOTTLE, PUMP
NDC Code 73740-4040-6
Package Description: 163 g in 1 BOTTLE, PUMP
Product Details
What is NDC 73740-4040?
What are the uses for Biosilk?
Which are Biosilk UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM (UNII: 7N6JUD5X6Y)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Biosilk 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)
- ANHYDROMETHYLENECITRIC ACID (UNII: 99197U4E9K)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- GLYCERIN (UNII: PDC6A3C0OX)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- SILK, ACID HYDROLYZED (1000 MW) (UNII: 8549W658QV)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CITRAL (UNII: T7EU0O9VPP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
What is the NDC to RxNorm Crosswalk for Biosilk?
- RxCUI: 1233282 - benzalkonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1233282 - benzalkonium chloride 1 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
[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".