Label: SCRUBS SUNSCREN- sunscreen lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 3, 2023

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  • Active Ingredients

    Active Ingredients

  • Purpose

    Sunscreen

    Sunscreen

    Sunscreen

    Sunscreen

  • Uses

    • helps prevent sunburn.
    • higher SPF gives more sunburn protection.
    • retains SPF after 80 minutes of water or sweating.
    • provides high protection against sunburn.
  • 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

    Stop use and ask a doctor rash or irritation develops and lasts

  • Keep out of reach of children

    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

    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours

  • Other Information

    Protect this product from excessive heat and direct sun.

    Sun alert: Limiting exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

  • Inactive Ingredients

    Inactive Ingredients

  • Questions and comments?

    Call: 1-877-684-5774

  • Package Label

    Sunscreen

  • INGREDIENTS AND APPEARANCE
    SCRUBS SUNSCREN 
    sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51239-3921
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.03 g  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.05 g  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE0.075 g  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.05 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PEG-6 SORBITAN OLEATE (UNII: 58O7V09UCI)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)  
    PROPYLENE GLYCOL PROPYL ETHER (UNII: 92KA3PYX0S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MEDIUM DENSITY POLYETHYLENE (UNII: 3W404QE89S)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51239-3921-1100 in 1 CARTON12/01/202105/06/2025
    17 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/01/202105/06/2025
    Labeler - ITW Pro Brands (067952994)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lico Industries098009041manufacture(51239-3921)
    Establishment
    NameAddressID/FEIBusiness Operations
    Prime Enterprises101946028manufacture(51239-3921) , analysis(51239-3921)
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