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

Available Formats

Dosage Form Package Information Links
POWDER 8 g in 1 CARTON (51346-041-01) Label Information

Complete UV LOCK ULTRA PACT SUN Information

  • ACTIVE INGREDIENT

    Active Ingredients: TITANIUM DIOXIDE 7.7%, ETHYLHEXYL METHOXYCINNAMATE 3%, ZINC OXIDE 2.9%


  • INACTIVE INGREDIENT

    Inactive Ingredients:
    MICA, TALC, SILICA, DIMETHICONE, NYLON-12, BISMUTH OXYCHLORIDE, MAGNESIUM STEARATE, TRIETHOXYCAPRYLYLSILANE, PHENYL METHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, LAUROYL LYSINE, SQUALANE, DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIISOSTEARYL MALATE, LANOLIN WAX, IRON OXIDES, ALUMINUM MYRISTATE, FRAGRANCE, METHICONE, METHYLPARABEN, ALLANTOIN, TOCOPHERYL ACETATE, 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, C9-15 FLUOROALCOHOL PHOSPHATE, PROPYLPARABEN, WATER, BUTYLENE GLYCOL


  • PURPOSE

    Purpose: Pact type sun block for UV ray protection, especially effective for touchup.


  • 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


  • DOSAGE AND ADMINISTRATION

    How to Use:
    Turn the cap a little to open, and hold the upper cover with the puff.
    Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.


  • INDICATIONS AND USAGE

    How to Use:
    Turn the cap a little to open, and hold the upper cover with the puff.
    Dispense an appropriate amount on the puff, and apply it to the entire face with a tapping motion.


  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    Image of carton


  • INGREDIENTS AND APPEARANCE
    UV LOCK ULTRA PACT SUN  SPF50PLUS PA PLUS PLUS PLUS
    titanium dioxide, octinoxate, zinc oxide powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51346-041
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.62 g  in 8 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 0.24 g  in 8 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.23 g  in 8 g
    Inactive Ingredients
    Ingredient Name Strength
    MICA (UNII: V8A1AW0880)  
    TALC (UNII: 7SEV7J4R1U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51346-041-01 8 g 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(51346-041)