NDC 71190-6487 Cc Cushion Compact Sunscreen - Light / Medium
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What is NDC 71190-6487?
What are the uses for Cc Cushion Compact Sunscreen - Light / Medium?
Which are Cc Cushion Compact Sunscreen - Light / Medium 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 CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Cc Cushion Compact 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)
- SHEA BUTTER (UNII: K49155WL9Y)
- JOJOBA OIL (UNII: 724GKU717M)
- CUCUMBER (UNII: YY7C30VXJT)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- CHAMOMILE (UNII: FGL3685T2X)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GLYCERIN (UNII: PDC6A3C0OX)
- DEXTRAN 40 (UNII: K3R6ZDH4DU)
- CAPROOYL TETRAPEPTIDE-3 (UNII: LZI0HJ3K2R)
- MANDELIC ACID (UNII: NH496X0UJX)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- TRIPLEUROSPERMUM INODORUM WHOLE (UNII: 567N54UG4S)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYALURONIC ACID (UNII: S270N0TRQY)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
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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".