Label: CALIFORNIA ALOE FRESH POW DERY SUN- homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick

  • NDC Code(s): 51346-532-01
  • Packager: NATURE REPUBLIC CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 18, 2024

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  • Drug Facts

  • Active Ingredients

    HOMOSALATE 9.0%
    OCTOCRYLENE 9.0%
    ETHYLHEXYL SALICYLATE 4.5%
    BUTYL METHOXYDIBENZOYLMETHANE 2.9%

  • Purpose

    Sunscreen

  • Uses

    Protects skin from direct sunlight and UV rays.

  • WARNINGS

    For external use only. Avoid contact with eyes. In the event of contact with eyes, rinse thoroughly with water. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace cap after use.

    Keep out of reach of children.

  • Directions

    Apply adequate amount of the product and thoroughly apply on the areas exposed to the UV rays. Apply the sunscreen product before exposure. Re-apply frequently to maintain protection, especially after perspiring, swimming or toweling.

  • Inactive Ingredients

    POLYETHYLENE, PROPYLHEPTYL CAPRYLATE, DIMETHICONE, SILICA, ISOPROPYL PALMITATE, METHYL METHACRYLATE CROSSPOLYMER, POLYMETHYLSILSESQUIOXANE, DICAPRYLYL CARBONATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, ACRYLATES COPOLYMER, OZOKERITE, FRAGRANCE, LAURYL PEG-8 DIMETHICONE, DEHYDROACETIC ACID, POLYGLYCERYL-2 TRIISOSTEARATE, TOCOPHEROL, YELLOW 5 LAKE(CI 19140), WATER, SEA WATER, BUTYLENE GLYCOL, PHENOXYETHANOL, ALOE BARBADENSIS LEAF EXTRACT, HIBISCUS ROSA-SINENSIS FLOWER/LEAF EXTRACT, MORINDA CITRIFOLIA EXTRACT, PENTYLENE GLYCOL, 1,2-HEXANEDIOL, CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN

  • PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    CALIFORNIA ALOE FRESH POW DERY SUN 
    homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51346-532
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE1.89 g  in 21 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1.89 g  in 21 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.94 g  in 21 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.6 g  in 21 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51346-532-0121 g in 1 CARTON; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/01/2020
    Labeler - NATURE REPUBLIC CO., LTD. (631172020)
    Registrant - NATURE REPUBLIC CO., LTD. (631172020)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kolmar Korea Co.,Ltd. Bucheon Factory963271763manufacture(51346-532)
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