NDC 53407-165 Reveal Color Correcting Anti-aging Serum Foundation Spf 15 Tan
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What is NDC 53407-165?
What are the uses for Reveal Color Correcting Anti-aging Serum Foundation Spf 15 Tan?
Which are Reveal Color Correcting Anti-aging Serum Foundation Spf 15 Tan UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Reveal Color Correcting Anti-aging Serum Foundation Spf 15 Tan 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)
- TALC (UNII: 7SEV7J4R1U)
- NYLON-12 (UNII: 446U8J075B)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- KARUM SEED OIL (UNII: 62160PU6FJ)
- UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
- DUNALIELLA SALINA (UNII: F4O1DKI9A6)
- APHANIZOMENON FLOS-AQUAE (UNII: 49VG1X560X)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- ISODODECANE (UNII: A8289P68Y2)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* Please review the disclaimer below.
[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".