Label: I CONCEAL FLAWLESS FOUNDATION BS SPF 30 SUNSCREEN SUEDE- zinc oxide and titanium dioxide cream
- NDC Code(s): 62742-4244-1, 62742-4244-2
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 10, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Directions • apply generously 15 minutes before sun exposure • children under 6 months of age: Ask a doctor • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • limit time in the sun, especially from 10 a.m.-2 p.m. • wear long-sleeved shirts, pants, hats and sunglasses
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients:
Water/Aqua/Eau, Cyclopentasiloxane, Coconut Alkanes, Squalane, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Glycerin, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Isohexadecane, Polyglyceryl-4 Isostearate, Vinyl Dimethicone/Lauryl Dimethicone, Crosspolymer, Hydrogen Dimethicone, Hydroxypropylcocoate PEG-8 Dimethicone, Dimethicone, Alumina, Polyglyceryl-3 Polydimthylsiloxyethyl Dimethicone, Cyclohexasiloxane, Magnesium Sulfate, Mica, Polyhydroxysteraic Acid, Phenoxyethanol, Triethoxysilyethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Caprylyl Glycol, Dimethicone/PEG-10/15 Crosspolymer, Ethylhexylglycerin, Hexylene Glycol, Dipotassium Glycyrrhizate, Perflurorodecalin, Zinc PCA, Saccharomyces Lysate Extract, Centella Asiatica Extract, Leuconostoc/Radish Root Ferment Filtrate, Olea Europea (Olive) Leaf Extract, Artemisia Vulgaris Extract , Hyaluronic Acid, Laminaria Digitata Extract, Phospholipids, Isomalt, Cyperus Rotundus Root Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Xanthium Sibiricum Fruit Extract, Dipropylene Glycol, Retinyl Palmitate, Tococpheryl Acetate, Opuntia Ficus-Indica Stem Extract, Sodium Citrate, Sodium Benzoate, Beta-Carotene, Potassium Sorbate, Salicylic Acid, Acetyl Hexapeptide-8, Sorbic Acid, Tocopherol, Lecithin, Vitis Vinifera (Grape) Fruit Cell Extract, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Ergothioneine, [+/ -: Bismuth Oxychloride (Ci 77163),Iron Oxide (Ci 77492), Iron Oxide (Ci 77491), Iron Oxide (Ci77499)]
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
I CONCEAL FLAWLESS FOUNDATION BS SPF 30 SUNSCREEN SUEDE
zinc oxide and titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4244 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 8.5 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 9.8 g in 100 g Inactive Ingredients Ingredient Name Strength ARTEMISIA VULGARIS WHOLE (UNII: JDR81QW9ZQ) HYALURONIC ACID (UNII: S270N0TRQY) LAMINARIA DIGITATA (UNII: 15E7C67EE8) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) COCONUT ALKANES (UNII: 1E5KJY107T) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) ISOMALT (UNII: S870P55O2W) OPUNTIA FICUS-INDICA STEM (UNII: MUD8892KHL) BETA CAROTENE (UNII: 01YAE03M7J) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) SQUALANE (UNII: GW89575KF9) POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y) GLYCERIN (UNII: PDC6A3C0OX) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA) HEXYLENE GLYCOL (UNII: KEH0A3F75J) HEXYL LAURATE (UNII: 4CG9F9W01Q) ISOHEXADECANE (UNII: 918X1OUF1E) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR) ALUMINUM OXIDE (UNII: LMI26O6933) POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q) CYCLOMETHICONE 6 (UNII: XHK3U310BA) MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) MICA (UNII: V8A1AW0880) PHENOXYETHANOL (UNII: HIE492ZZ3T) TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE (UNII: X75PL53TZJ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) PERFLUNAFENE (UNII: 54A06VV62N) ZINC PIDOLATE (UNII: C32PQ86DH4) SACCHAROMYCES LYSATE (UNII: R85W246Z1C) XANTHIUM SIBIRICUM FRUIT (UNII: 3H333L84C2) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM BENZOATE (UNII: OJ245FE5EU) SALICYLIC ACID (UNII: O414PZ4LPZ) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SORBIC ACID (UNII: X045WJ989B) TOCOPHEROL (UNII: R0ZB2556P8) WINE GRAPE (UNII: 3GOV20705G) ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) HYDROXYPROPYLCOCOATE PEG-8 DIMETHICONE (UNII: 8TE0BZU36S) DIMETHICONE (UNII: 92RU3N3Y1O) DIPROPYLENE GLYCOL (UNII: E107L85C40) CYPERUS ROTUNDUS ROOT (UNII: 4B51SRR959) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ERGOTHIONEINE (UNII: BDZ3DQM98W) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4244-2 1 in 1 CARTON 01/10/2024 1 NDC:62742-4244-1 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/10/2024 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4244)