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Laneige UV TOTAL BASE (AMOREPACIFIC)

Available Formats

Dosage Form Package Information Links
LOTION 1 TUBE in 1 CARTON (43419-861-25) > 50 mL in 1 TUBE Label Information

Complete Laneige UV TOTAL BASE Information

  • WARNING LABEL

    FOR EXTERNAL USE ONLY.

    AVOID CONTACT WITH EYES. DISCONTINUE USE IF SIGNS OF IRRITATION APPEAR.

    KEEP OUT OF REACH OF CHILDREN.


  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS

    EHYLHEXYL METHOXYNNAMATE 7.00%, TITANIUM DIOXIDE 8.40%, ZINC OXIDE 2.00%


  • INDICATIONS & USAGE

    Triple functional total base serving as UV protecting, makeup base and foundation

    Dermatologist Tested

    50ml / 1.7 FL.OZ. e


  • INGREDIENTS

    OZOKERITE, SQUALANE/CALCIUM STEARATE/SORBITAN-SESQUIOLEATE, DICAPRYLYL CARBONATE, ETHYLHEXYL METHOOXYCINNAMATE, METHYLPARABEN, PROPYLPARABEN, DISTEARDIMONIUM HECTORITE, CETYL PEG.PPG-10.1 DIMETHICONE (CETYL DIMETHICONE COPOLYOL), SORBITAN ISOSTEARATE, METHYL TRIMETHICONE, DECAMETHYL CYCLOPENTASILOXANE (CYCLOMETHICONE), CYCLOPENTASILOXANE/POLYSILICONE-11/DIMETHICONE, VINYL DIMETHICONE.METHICONE SILSESQUIOXANE CROSSPOLYMER, ZINC OXIDE, TITANIUM DIOXIDE, IRON OXIDES, POLYMETHYL METHACRYLATE, SYSTHETIC FLUORPHLOGOPITE/TRIEHTOXYCAPRYLYLSILANE, TITANATED MICA, WATER, ALGAE EXTRACT (WATER/LAMINARIA DIGITATA EXTRACT), WATER/BUTYLENE GLYCOL/BEESWAX/POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE/HYDROXYPROPYL BISPALMITAMIDE MEA/INULIN LAURYL CARBAMATE, BUTYLENE GLYCOL, SODIUM CHLORIDE, DISODIUM EDTA, PERFUME


  • SPL UNCLASSIFIED SECTION

    AMOREPACIFIC US INC.
    270 Sylvan Ave. #255
    Englewood Cliffs, NJ 07632

    www.laneige.com


  • PRINCIPAL DISPLAY PANEL - 50ml Tube Carton

    LANEÍGE

    UV TOTAL BASE
    SPF40 PA++

    50ml / 1.7 FL.OZ.

    Principal Display Panel - 50ml Tube Carton

  • INGREDIENTS AND APPEARANCE
    LANEIGE UV TOTAL BASE 
    octinoxate, titanium dioxide, and zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43419-861
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate .07 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE .084 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE .02 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    SQUALANE (UNII: GW89575KF9)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    MICA (UNII: V8A1AW0880)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CALCIUM STEARATE (UNII: 776XM7047L)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43419-861-25 1 in 1 CARTON
    1 50 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 09/15/2010
    LANEIGE UV TOTAL BASE 
    octinoxate, titanium dioxide, and zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43419-862
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate .07 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE .084 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE .02 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    SQUALANE (UNII: GW89575KF9)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    MICA (UNII: V8A1AW0880)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CALCIUM STEARATE (UNII: 776XM7047L)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43419-862-26 1 in 1 CARTON
    1 50 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 09/15/2010
    Labeler - AMOREPACIFIC (687995683)
    Establishment
    Name Address ID/FEI Business Operations
    AMOREPACIFIC 687995683 MANUFACTURE