Label: BRUSHONBLOCK MINERAL POWDER SUNSCREEN BROAD SPECTRUM SPF30 TRANSLUCENT- avobenzone, octinoxate, octisalate, octocrylene cream

  • NDC Code(s): 84255-000-00
  • Packager: Brownkind Dermascience Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 10, 2024

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredients

    Avobenzone 2.5%

    Octinoxate 7.5%

    Octisalate 5%

    Octocrylene 1%

    Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • if used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
  • Warnings

    For external use only

    Do not use 

    • on damaged or broken skin

    When using this product

    • keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor if

    • rash occurs

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply liberally 15 minutes before sun exposure.
    • Reapply at least every 2 hours.
    • Use a water-resistant sunscreen if swimming or sweating. Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10AM-2PM
    • wear long-sleeved shirts, pants, hats, and sunglasses
    • children under 6 months of age: ask a doctor.
  • Other Information

    Protect the product in this container from excessive heat and direct sunlight.

  • Inactive Ingredients

    Water, Octocrylene, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Glyceryl Stearate, Diethylhexyl 2,6-Naphthalate, Ceteareth-20, Calcium Sodium Borosilicate, Butyl Methoxydibenzoylmethane, Niacinamide, Glycerin, Butylene Glycol, PEG-10 Stearate, Magnesium Aluminum Silicate, Cetearyl Alcohol, VP/Hexadecene Copolymer, Phenoxyethanol, Propanediol, Polymethylsilsesquioxane, Dimethicone, Isohexadecane, Xanthan Gum, Octyldodecanol, Glyceryl Stearate SE, Cetearyl Methicone, PEG-40 Stearate, Steareth-2, Steareth-21,Ethylhexylglycerin, Disodium EDTA, Amla (Phyllanthus Emblica) Fruit Extract, BHT, Rainbow Algae (Cystoseira Tamariscifolia) Extract, Cocoa (Theobroma Cacao) Extract, Lecithin, Tocopherol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Sodium Benzoate 

  • Questions?

    1(800) 687-7165

  • Package Labelling:

    Label.jpgInner Label.jpg

  • INGREDIENTS AND APPEARANCE
    BRUSHONBLOCK MINERAL POWDER SUNSCREEN BROAD SPECTRUM SPF30 TRANSLUCENT 
    avobenzone, octinoxate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84255-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PEG-10 STEARATE (UNII: D3AHD468TV)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    STEARETH-2 (UNII: V56DFE46J5)  
    STEARETH-21 (UNII: 53J3F32P58)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    COCOA (UNII: D9108TZ9KG)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84255-000-001 in 1 CARTON06/01/2024
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/01/2024
    Labeler - Brownkind Dermascience Inc. (119235137)