NDC 73740-5003 Biosilk Pomegranite
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 73740-5003?
What are the uses for Biosilk Pomegranite?
Which are Biosilk Pomegranite 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 Pomegranite 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:
- DIMETHICONE 1000 (UNII: MCU2324216)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SILK, ENZYME HYDROLYZED (1000 MW) (UNII: 960MDR3Z07)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ALCOHOL (UNII: 3K9958V90M)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- CITRAL (UNII: T7EU0O9VPP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- C15-19 ALKANE (UNII: CI87N1IM01)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
What is the NDC to RxNorm Crosswalk for Biosilk Pomegranite?
- RxCUI: 1046442 - benzalkonium chloride 0.13 % Topical Lotion
- RxCUI: 1046442 - benzalkonium chloride 1.3 MG/ML Topical Lotion
* 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".