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UV LOCK ULTRA MILK SUN (NATURE REPUBLIC CO., LTD.)

Available Formats

Dosage Form Package Information Links
CREAM 50 mL in 1 CARTON (51346-042-01) Label Information

Complete UV LOCK ULTRA MILK SUN Information

  • ACTIVE INGREDIENT

    Active Ingredients: ETHYLHEXYL METHOXYCINNAMATE 7.5%, ZINC OXIDE 6.5%, ETHYLHEXYL SALICYLATE 5%, TITANIUM DIOXIDE 2.5%


  • INACTIVE INGREDIENT

    Inactive Ingredients:
    WATER, CYCLOPENTASILOXANE, ALCOHOL,BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, ISODECYL NEOPENTANOATE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, MAGNESIUM SULFATE, PHENOXYETHANOL, CALCIUM ALUMINUM BOROSILICATE, FRAGRANCE, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, SILICA, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, POLYGLYCERYL-6 POLYRICINOLEATE, OPUNTIA FICUS-INDICA EXTRACT, PORTULACA OLERACEA EXTRACT, ARNICA MONTANA FLOWER EXTRACT, CENTAUREA CYANUS FLOWER EXTRACT, DIANTHUS CARYOPHYLLUS FLOWER EXTRACT, FREESIA REFRACTA EXTRACT, IRIS VERSICOLOR EXTRACT, JASMINUM OFFICINALE (JASMINE) FLOWER/LEAF EXTRACT, ZANTEDESCHIA AETHIOPICA FLOWER/STEM EXTRACT, CELLULOSE GUM, MICROCRYSTALLINE CELLULOSE


  • PURPOSE

    Purpose: Strong milk sun block with daily skincare effects.


  • WARNINGS


    Cautions:
    For external use only.
    Avoid contact with eyes and mouth.
    Discontinue use if signs of irritation or rash appear.
    Keep out of reach of children.
    Replace the cap after use.


  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN


  • INDICATIONS AND USAGE

    How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.


  • DOSAGE AND ADMINISTRATION

    How to Use: Shake 3-5 times before use. Evenly apply an appropriate amount to skin that is exposed to UV rays.


  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    Image of carton


  • INGREDIENTS AND APPEARANCE
    UV LOCK ULTRA MILK SUN  SPF50PLUS PA PLUS PLUS PLUS
    octinoxate, zinc oxide, octisalate, titanium dioxide cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-042
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3.75 g  in 50 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 3.25 g  in 50 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.50 g  in 50 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1.25 g  in 50 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51346-042-01 50 mL in 1 CARTON
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 01/02/2012
    Labeler - NATURE REPUBLIC CO., LTD. (631172020)
    Registrant - NATURE REPUBLIC CO., LTD. (631172020)
    Establishment
    Name Address ID/FEI Business Operations
    NATURE REPUBLIC CO., LTD. 631172020 manufacture(51346-042)