NDC 41442-123 Complexion Brightener Spf20
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 41442-123?
What are the uses for Complexion Brightener Spf20?
Which are Complexion Brightener Spf20 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 Complexion Brightener Spf20 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:
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- GLYCERIN (UNII: PDC6A3C0OX)
- SQUALANE (UNII: GW89575KF9)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
- ALCOHOL (UNII: 3K9958V90M)
- MICA (UNII: V8A1AW0880)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- NIACINAMIDE (UNII: 25X51I8RD4)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- RORIPPA NASTURTIUM-AQUATICUM FLOWERING TOP (UNII: W1N2U8I64G)
- ACEROLA (UNII: XDD2WEC9L5)
- APPLE (UNII: B423VGH5S9)
- PECTIN (UNII: 89NA02M4RX)
- APRICOT SEED OIL (UNII: 54JB35T06A)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LACTIC ACID (UNII: 33X04XA5AT)
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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".