NDC 11489-087 No7 Lift And Luminite Day Cream Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 11489-087?
What are the uses for No7 Lift And Luminite Day Cream Spf 15?
Which are No7 Lift And Luminite Day Cream Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are No7 Lift And Luminite Day Cream Spf 15 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- SHEA BUTTER (UNII: K49155WL9Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MICA (UNII: V8A1AW0880)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- ETHYLPARABEN (UNII: 14255EXE39)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LUPINUS ALBUS SEED (UNII: 24GB753W3B)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- BIOTIN (UNII: 6SO6U10H04)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".