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QUINCE WHITENING SUN (SKINFOOD CO., LTD.)

Available Formats

Dosage Form Package Information Links
LOTION 70 mL in 1 BOTTLE (76214-031-01) Label Information

Complete QUINCE WHITENING SUN Information

  • ACTIVE INGREDIENT

    Active ingredients: OCTINOXATE 7.0%, OCTISALATE 5.0%, TITANIUM DIOXIDE 0.93%


  • INACTIVE INGREDIENT

    Inactive ingredients:
    WATER, ISOAMYL p-METHOXYCINNAMATE, BUTYLENE GLYCOL, PROPYLENE GLYCOL, ARBUTIN, CETEARETH-6 OLIVATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, C14-22 ALCOHOLS, CYCLOPENTASILOXANE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, SORBITAN STEARATE, C12-20 ALKYL GLUCOSIDE, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, BRASSICA OLERACEA ITALICA (BROCCOLI) EXTRACT, CHAENOMELES SINENSIS FRUIT EXTRACT, HONEY EXTRACT, ISOHEXADECANE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER, POLYSORBATE 80, POTASSIUM CETYL PHOSPHATE, DISODIUM EDTA, ALUMINUM HYDROXIDE, STEARIC ACID, BHT, TOCOPHERYL ACETATE, PROPYLPARABEN, PHENOXYETHANOL, METHYLPARABEN, FRAGRANCE, SILICA


  • PURPOSE

    Purpose: Protects skin from UV rays.


  • WARNINGS

    Warnings:
    For external use only.
    Avoid contact with eyes.
    Discontinue use if signs of irritation appear.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:
    Keep out of reach of children.


  • INDICATIONS & USAGE

    Indication and usage:
    Use at the end of your daily skincare regimen.
    Apply liberally onto face and body before sun exposure avoiding the eye area.


  • DOSAGE & ADMINISTRATION

    Dosage and administration:
    For best results, apply at least 15 to 20 minutes before sun exposure.
    Reapply frequently while out in the sun.


  • INGREDIENTS AND APPEARANCE
    QUINCE WHITENING SUN  SPF 34 PA PLUS PLUS
    octinoxate lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:76214-031
    Route of Administration CUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 4.9 mL  in 70 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 3.5 mL  in 70 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 0.65 mL  in 70 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ARBUTIN (UNII: C5INA23HXF)  
    C14-22 ALCOHOLS (UNII: B1K89384RJ)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BROCCOLI (UNII: UOI4FT57BZ)  
    CHAENOMELES SPECIOSA FRUIT (UNII: 6S5Q1Q537Z)  
    HONEY (UNII: Y9H1V576FH)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:76214-031-01 70 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 03/01/2011
    Labeler - SKINFOOD CO., LTD. (690324173)
    Registrant - SKINFOOD CO., LTD. (690324173)
    Establishment
    Name Address ID/FEI Business Operations
    SKINFOOD CO., LTD. 690324173 manufacture