NDC 68828-192 Cc Cream Complexion Corrector Medium Dark Broad Spectrum Spf 15 Jafra
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68828-192?
What are the uses for Cc Cream Complexion Corrector Medium Dark Broad Spectrum Spf 15 Jafra?
Which are Cc Cream Complexion Corrector Medium Dark Broad Spectrum Spf 15 Jafra 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Cc Cream Complexion Corrector Medium Dark Broad Spectrum Spf 15 Jafra 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)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- HYDROXYPROPYLCOCOATE PEG-8 DIMETHICONE (UNII: 8TE0BZU36S)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SQUALANE (UNII: GW89575KF9)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- LAUROYL LYSINE (UNII: 113171Q70B)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- UNDECYLENOYL GLYCINE (UNII: 4D20464K2J)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CUCUMBER (UNII: YY7C30VXJT)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- 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".