Label: ARUBA SUN SPF 30 SUNSCREEN- avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 6% lotion

  • NDC Code(s): 72839-137-08, 72839-137-18, 72839-137-28, 72839-137-38
  • Packager: Derma Care Research Labs,LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 5, 2024

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  • Active Ingredients

    Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 6%

  • 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 eyes 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:

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

    Sun protection measures: spending time n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including:

    • limit time in the sun, especially from 10 am to 2 pm
    • wear long-sleeved shirts, pants, hats, and sunglasses.
    • Children under 6 months: ask a doctor.

  • Inactive Ingredients

    Water, Sorbitol, Aluminum Starch Octenylsuccinate, VP/Eicosene Copolymer, Stearic Acid, Dimethicone, Tocopherol, Ethylhexylglycerin, Phenoxyethanol, Polyglyceryl-3 Distearate, Sorbitan Isostearate, Carbomer, Disodium EDTA, Triethanolamine, Benzyl Alcohol, Fragrance.

  • Label

    Aruba Sun SPF 30 Sunscreen, 8 oz, NDC 72839-137-08

    LABEL

    Bonaire Sun SPF 30 Sunscreen Lotion, 8oz, NDC 72839-137-18

    LABEL

    Curacao Sun SPF 30 Sunscreen Lotion, 8 oz, NDC 72839-137-28

    LABELAntigua Sun SPF 30 Sunscreen Lotion, 8 oz, NDC 72839-137-38

    LABEL

  • INGREDIENTS AND APPEARANCE
    ARUBA SUN SPF 30 SUNSCREEN 
    avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 6% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-137
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE6 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    SORBITOL (UNII: 506T60A25R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72839-137-08227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/25/2021
    2NDC:72839-137-18227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/15/2022
    3NDC:72839-137-28227 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product12/15/2022
    4NDC:72839-137-38227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/25/2021
    Labeler - Derma Care Research Labs,LLC (116817470)
    Registrant - Derma Care Research Labs, LLC (116817470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Derma Care Research Labs116817470manufacture(72839-137)
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