NDC 59779-301 Age Renewal Firming And Hydrating Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Woonsocket Prescription Center, Incorporated
- 59779-301 - Age Renewal Firming And Hydrating Moisturizer
Product Packages
NDC Code 59779-301-01
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 51 g in 1 BOTTLE, GLASS
Product Details
What is NDC 59779-301?
Which are Age Renewal Firming And Hydrating Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Age Renewal Firming And Hydrating Moisturizer 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SQUALANE (UNII: GW89575KF9)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- RETINOL (UNII: G2SH0XKK91)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ARGININE (UNII: 94ZLA3W45F)
- SOYBEAN (UNII: L7HT8F1ZOD)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- PICEA ABIES WOOD (UNII: 72GZ8K8996)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- BENTONITE (UNII: A3N5ZCN45C)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SORBITOL (UNII: 506T60A25R)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PANTHENOL (UNII: WV9CM0O67Z)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".