NDC 67938-2062 Flawless Finish Perfectly Satinb 24hr Makeup Shade Sunbeige
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 67938-2062?
What are the uses for Flawless Finish Perfectly Satinb 24hr Makeup Shade Sunbeige?
Which are Flawless Finish Perfectly Satinb 24hr Makeup Shade Sunbeige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Flawless Finish Perfectly Satinb 24hr Makeup Shade Sunbeige 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MICA (UNII: V8A1AW0880)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISODODECANE (UNII: A8289P68Y2)
- NYLON-12 (UNII: 446U8J075B)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- ALCOHOL (UNII: 3K9958V90M)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LAUROYL LYSINE (UNII: 113171Q70B)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
- BAMBUSA BAMBOS STEM (UNII: NRA4497HC5)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".