NDC 82439-103 Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light/medium
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82439-103?
What are the uses for Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light/medium?
Which are Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light/medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Bff Skin Perfector Spf 30 Broad Spectrum Sunscreen Light/medium 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- STEARETH-21 (UNII: 53J3F32P58)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PROPANEDIOL (UNII: 5965N8W85T)
- .BETA.-GLUCOGALLIN (UNII: 4X7JGS9BFY)
- ZEIN (UNII: 80N308T1NN)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- STEARETH-2 (UNII: V56DFE46J5)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- DIMETHYLMETHOXY CHROMANOL (UNII: XBH432G01F)
- STARCH, CORN (UNII: O8232NY3SJ)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- SUCCINIC ACID (UNII: AB6MNQ6J6L)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- COCONUT (UNII: 3RT3536DHY)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- BORON NITRIDE (UNII: 2U4T60A6YD)
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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".