NDC 81488-006 Puriton Perfect Brightening Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81488-006?
What are the uses for Puriton Perfect Brightening Sunscreen?
Which are Puriton Perfect Brightening Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Puriton Perfect Brightening Sunscreen 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:
- ADENOSINE (UNII: K72T3FS567)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)
- BENZYL BENZOATE (UNII: N863NB338G)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CINNAMYL ALCOHOL (UNII: SS8YOP444F)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- COUMARIN (UNII: A4VZ22K1WT)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GERANIOL (UNII: L837108USY)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ADANSONIA DIGITATA SEED (UNII: 2936P60TPX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPANEDIOL (UNII: 5965N8W85T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- AMINO ACIDS, SILK (UNII: V0L00EX1IA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".