NDC 73740-7070 Biosilk
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 73740-7070?
What are the uses for Biosilk?
Which are Biosilk UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- 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:
- PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
- COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ALCOHOL (UNII: 3K9958V90M)
- EDETIC ACID (UNII: 9G34HU7RV0)
- BENZYL BENZOATE (UNII: N863NB338G)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- AMINO ACIDS, SILK (UNII: V0L00EX1IA)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- PROPANEDIOL (UNII: 5965N8W85T)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- COUMARIN (UNII: A4VZ22K1WT)
What is the NDC to RxNorm Crosswalk for Biosilk?
- RxCUI: 1665365 - benzalkonium chloride 0.1 % Medicated Shampoo
- RxCUI: 1665365 - benzalkonium chloride 1 MG/ML Medicated Shampoo
* 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".