NDC 68078-018 Mattifying Perfector Spf 20 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68078-018?
What are the uses for Mattifying Perfector Spf 20 Sunscreen?
Which are Mattifying Perfector Spf 20 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mattifying Perfector Spf 20 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- ETHYLHEXYL HYDROXYSTEARATE BENZOATE (UNII: 3W8F25684B)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- WATER (UNII: 059QF0KO0R)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- RICE BRAN (UNII: R60QEP13IC)
- OAT (UNII: Z6J799EAJK)
- SPIRULINA MAXIMA (UNII: 9K7IG15M0Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DULSE (UNII: 7832HOY4ZQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYSACCHARIDE-K (UNII: 3X48A86C8K)
- JOJOBA OIL (UNII: 724GKU717M)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TEA TREE OIL (UNII: VIF565UC2G)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MANDARIN OIL (UNII: NJO720F72R)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- CANANGA OIL (UNII: 8YOY78GNNX)
- CYMBOPOGON SCHOENANTHUS OIL (UNII: XE7K568ILO)
- CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- MICA (UNII: V8A1AW0880)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CITRAL (UNII: T7EU0O9VPP)
- FARNESOL (UNII: EB41QIU6JL)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
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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".