NDC 11489-117 No7 Lift And Luminate Triple Action Day Cream Spf 30
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Product Details
What is NDC 11489-117?
What are the uses for No7 Lift And Luminate Triple Action Day Cream Spf 30?
Which are No7 Lift And Luminate Triple Action Day Cream Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are No7 Lift And Luminate Triple Action Day Cream Spf 30 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)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MICA (UNII: V8A1AW0880)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIMETHICONOL (40 CST) (UNII: 343C7U75XW)
- ETHYLPARABEN (UNII: 14255EXE39)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- N-ACETYL DIPEPTIDE-1 (UNII: HA41Z1UF8D)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MORUS ALBA LEAF (UNII: M8YIA49Q2P)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
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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".