NDC 59779-339 Antibacterial Moisturizing Hand Lotion Sun Blossom
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What is NDC 59779-339?
What are the uses for Antibacterial Moisturizing Hand Lotion Sun Blossom?
Which are Antibacterial Moisturizing Hand Lotion Sun Blossom UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Moisturizing Hand Lotion Sun Blossom 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:
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SOYBEAN OIL (UNII: 241ATL177A)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- MICA (UNII: V8A1AW0880)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- AVOBENZONE (UNII: G63QQF2NOX)
- OCTISALATE (UNII: 4X49Y0596W)
- POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Antibacterial Moisturizing Hand Lotion Sun Blossom?
- RxCUI: 1102185 - benzalkonium chloride 0.1 % Topical Lotion
- RxCUI: 1102185 - benzalkonium chloride 1 MG/ML Topical Lotion
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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".