Label: ARUBA ALOE VERY WATER RESISTANT SUNSCREEN SPF 15- octinoxate, oxybenzone lotion

  • NDC Code(s): 53675-155-02, 53675-155-06
  • Packager: Aruba Aloe Balm, NV
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2023

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

  • Active Ingredients

    Octinoxate 7.5% Oxybenzone 4.5%

  • Purpose

    Sunscreen

  • Uses

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

    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, Aruba Aloe Vera gel, VP/Eicosene Copolymer, stearic acid, cetyl phosphate, cetearyl alcohol, coconut oil, jojoba oil, tocopheryl acetate (Vitamin E Acetate), myristyl myristate, dimethicone, carbomer 934, phenoxyethanol, ethlparabven, methylparaben, propylparaben, triethanolamine, fragrance

  • SPL UNCLASSIFIED SECTION

    www.arubaaloe.com

    Made in Aruba by Aruba Aloe Balm, Inc

    PO Box 360, Aruba Dutch Caribbean. Distributed in the USA by Aruba Aloe of North America, LLC, Indianapolis, IN 46244. Customer inquiry Hotline: 1-800-95 ARUBA


  • Description

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

  • PRINCIPAL DISPLAY PANEL

    ARUBA ALOE

    since 1890

    Very Water Resistant

    Sunscreen SPF 15

    Made in Aruba with the Worlds Finest Aloe (tm)


  • PRINCIPAL DISPLAY PANEL

    Aruba Aloe Sunscreen

  • INGREDIENTS AND APPEARANCE
    ARUBA ALOE VERY WATER RESISTANT SUNSCREEN   SPF 15
    octinoxate, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53675-155
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE45 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 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:53675-155-0265 mL in 1 BOTTLE; Type 0: Not a Combination Product07/08/2011
    2NDC:53675-155-06177 mL in 1 BOTTLE; Type 0: Not a Combination Product07/08/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/08/2011
    Labeler - Aruba Aloe Balm, NV (855442273)