NDC 53407-170 Sublime Defense Anti-aging Blurring Moisturizer Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53407 - Terravia, Inc.
- 53407-170 - Sublime Defense Anti-aging Blurring Moisturizer Spf 30
Product Packages
NDC Code 53407-170-60
Package Description: 1 JAR in 1 BOX / 60 mL in 1 JAR
NDC Code 53407-170-61
Package Description: 1 JAR in 1 BOX / 7 mL in 1 JAR
Product Details
What is NDC 53407-170?
What are the uses for Sublime Defense Anti-aging Blurring Moisturizer Spf 30?
Which are Sublime Defense Anti-aging Blurring Moisturizer Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sublime Defense Anti-aging Blurring Moisturizer Spf 30 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)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- SQUALANE (UNII: GW89575KF9)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- GINGER (UNII: C5529G5JPQ)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- CHICORY ROOT (UNII: 090CTY533N)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SODIUM C14 OLEFIN SULFONATE (UNII: N816E2SOKI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- FERROUS OXIDE (UNII: G7036X8B5H)
* 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".