NDC 62742-4175 I Conceal Flawless Foundation Broad Spectrum Spf 30 Sunscreen Suede
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4175 - I Conceal Flawless Foundation Broad Spectrum Spf 30 Sunscreen Suede
Product Packages
NDC Code 62742-4175-2
Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE (62742-4175-1)
Product Details
What is NDC 62742-4175?
What are the uses for I Conceal Flawless Foundation Broad Spectrum Spf 30 Sunscreen Suede?
Which are I Conceal Flawless Foundation Broad Spectrum Spf 30 Sunscreen Suede UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are I Conceal Flawless Foundation Broad Spectrum Spf 30 Sunscreen Suede 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)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- TETRADECANE (UNII: 03LY784Y58)
- MICA (UNII: V8A1AW0880)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- PERFLUNAFENE (UNII: 54A06VV62N)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ARTEMISIA VULGARIS WHOLE (UNII: JDR81QW9ZQ)
- HYALURONIC ACID (UNII: S270N0TRQY)
- ISOMALT (UNII: S870P55O2W)
- CYPERUS ROTUNDUS TUBER (UNII: 4B51SRR959)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- XANTHIUM SIBIRICUM FRUIT (UNII: 3H333L84C2)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- SORBIC ACID (UNII: X045WJ989B)
- WINE GRAPE (UNII: 3GOV20705G)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BETA CAROTENE (UNII: 01YAE03M7J)
* 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".