Label: ARUBA ALOE VERY WATER RESISTANT SUNSCREEN - FOR FACES SPF 30- homosalate, octinoxate, padimate o, oxybenzone lotion

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

Drug Label Information

Updated November 14, 2023

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  • Active Ingredients

    Homosalate 8.0%

    Octinoxate 7.0%

    Padimate O 4.2%

    Oxybenzone 3.0%

  • Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • Higher SPF gives more sunburn protection
    • Retains SPF after 80 minutes of activity in the water or perspiring
  • Warnings

    For external use only.

    When using this product

    keep out of eyes, rinse with water to remove.

    Stop using and ask a doctor

    if rash or irritation develops and lasts

    Keep out of reach of children

  • Directions

    • Apply generously before sun exposure and as needed
    • Children under 6 months of age; ask a doctor.
  • Inactive Ingredients

    Water, Aloe Vera Gel (from Aruba), VP/Eicosene Copolymer, Stearic Acid, Cetyl Phosphate, Cetearyl Alcohol, Coconut Oil, Jojoba Oil, Tocopheryl Acetate (Vitamin E Acetate), Myristyl Myristate, Dimethicone, Carbomer 934, Phenoxyethanol, Ethylparaben, Methylparaben, Propylparaben, Triethanolamine, Fragrance

  • PRINCIPAL DISPLAY PANEL

    Aruba Aloe

    Since 1890

    Very Water Resistant

    Sunscreen

    SPF 30 FOR FACES

    Made In Aruba

    World's Finest Aloe

    4.2oz (e124mL)



    Our unique, lightweight formulation is readily absorbed into the skin and provides protection from the suns harmful rays. Formulated especially for sensitive facial skin, it will soothe and moisturize while protecting the skin.

    Shop. Browse, Learn. Www. ArubaAloe.com



    This bottle contains 100% post consumer recycled plastic. Please recycle. Aruba Aloe products are not tested on animals.

  • PRINCIPAL DISPLAY PANEL

    Aruba Aloe Sunscreen

  • INGREDIENTS AND APPEARANCE
    ARUBA ALOE VERY WATER RESISTANT SUNSCREEN - FOR FACES  SPF 30
    homosalate, octinoxate, padimate o, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53675-154
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE80 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE70 mg  in 1 mL
    PADIMATE O (UNII: Z11006CMUZ) (PADIMATE O - UNII:Z11006CMUZ) PADIMATE O42 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETYL PHOSPHATE (UNII: VT07D6X67O)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    JOJOBA OIL (UNII: 724GKU717M)  
    ACETATE ION (UNII: 569DQM74SC)  
    MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CARBOMER 934 (UNII: Z135WT9208)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53675-154-04124 mL in 1 JAR; Type 0: Not a Combination Product07/06/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/06/2011
    Labeler - Aruba Aloe Balm NV (855442273)
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