NDC 59779-331 Moisturizing Hand Citrus Coconut
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-331 - Moisturizing Hand
Product Packages
NDC Code 59779-331-03
Package Description: 72 mL in 1 TUBE
Product Details
What is NDC 59779-331?
What are the uses for Moisturizing Hand Citrus Coconut?
Which are Moisturizing Hand Citrus Coconut UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Moisturizing Hand Citrus Coconut 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)
- COCONUT (UNII: 3RT3536DHY)
- LEMON (UNII: 24RS0A988O)
- 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)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Moisturizing Hand Citrus Coconut?
- RxCUI: 1102185 - benzalkonium chloride 0.1 % Topical Lotion
- RxCUI: 1102185 - benzalkonium chloride 1 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".