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UV LOCK FLOWER NON CHEMICAL SUN (NATURE REPUBLIC CO., LTD.)

Available Formats

Dosage Form Package Information Links
LIQUID 50 mL in 1 CARTON (51346-212-01) Label Information

Complete UV LOCK FLOWER NON CHEMICAL SUN Information

  • ACTIVE INGREDIENT

    Active Ingredients: ZINC OXIDE 12.48%, TITANIUM DIOXIDE 2%


  • INACTIVE INGREDIENT

    Inactive Ingredients:
    CYCLOPENTASILOXANE, WATER, BUTYLENE GLYCOL, DICAPRYLYL CARBONATE, NIACINAMIDE, METHYL METHACRYLATE CROSSPOLYMER, PEG-10 DIMETHICONE, PORTULACA OLERACEA EXTRACT, DIMETHICONE, MAGNESIUM SULFATE, METHICONE, BIOSACCHARIDE GUM-1, POLYMETHYL METHACRYLATE, SILICA, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PHENOXYETHANOL, ALUMINUM HYDROXIDE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, CALCIUM ALUMINUM BOROSILICATE, CAPRYLYL GLYCOL, FRAGRANCE, STEARIC ACID, ALOE BARBADENSIS LEAF JUICE, ANTHEMIS NOBILIS FLOWER EXTRACT, GLYCERYL CAPRYLATE, HAMAMELIS VIRGINIANA FLOWER WATER, NELUMBO NUCIFERA FLOWER WATER, POLYGLYCERYL-6 POLYRICINOLEATE, TOCOPHERYL ACETATE, MICROCRYSTALLINE CELLULOSE, ADENOSINE, CELLULOSE GUM, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL


  • PURPOSE

    Purpose: Sunscreen


  • WARNINGS

    Cautions:
    For external use only.
    Avoid contact with eyes and mouth.
    Discontinue use if signs of irritation or rashes 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: Gently shake the bottle 3-5 times before use, and evenly apply an appropriate amount to skin that can be easily exposed to UV rays.


  • DOSAGE AND ADMINISTRATION

    How to Use: Gently shake the bottle 3-5 times before use, and evenly apply an appropriate amount to skin that can be easily exposed to UV rays.


  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    Image of carton


  • INGREDIENTS AND APPEARANCE
    UV LOCK FLOWER NON CHEMICAL SUN  SPF50PLUS PA PLUS PLUS PLUS
    zinc oxide, titanium dioxide liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-212
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 6.24 mg  in 50 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 1 mg  in 50 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51346-212-01 50 mL in 1 CARTON
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 02/01/2013
    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(51346-212)