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Ocean Potion 50 Instant Dry Kid Spotstick (Sun & Skin Care Research, LLC)

Available Formats

Dosage Form Package Information Links
LIQUID 19 mL in 1 BOTTLE, WITH APPLICATOR (62802-581-01) Label Information

Complete Ocean Potion 50 Instant Dry Kid Spotstick Information

  • Active Ingredients


    Homosalate: 15%
    Octisalate: 5%
    Octocrylene: 7%
    Avobenzone: 3%



  • Purpose

    Sunscreen


  • Uses

    • helps prevent sunburn
    • If used as directed with other skin 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. Stop use and ask a doctor if rash occurs. When using this product keep out of eyes. Rinse with water to remove. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.  Flammable  Do not use near heat or open flames.  Keep treated skin away from fire, sparks or flames until dry.


  • Directions

    • Apply liberally 15 minutes before sun exposure, depress sponge top to initiate product application
    • reapply after 80 minutes of swimming or sweating and immediately after towel drying
    • at least every 2 hours
    • 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 limiting time in the sun, especially from 10a.m.-2p.m., wear long-sleeved shirts, pants hats and sunglasses.
    • children under 6 months: Ask a doctor

  • Other Information

    • For use on skin only
    • Avoid contact with fabric
    • Protect this product from excessive heat and direct sun

  • INGREDIENTS AND APPEARANCE
    OCEAN POTION 50 INSTANT DRY KID SPOTSTICK  
    avobenzone, homosalate, octisalate, octocrylene liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:62802-581
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 15 mL  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 mL  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 7 mL  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62802-581-01 19 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 01/01/2012
    Labeler - Sun & Skin Care Research, LLC (849772207)
    Establishment
    Name Address ID/FEI Business Operations
    Sun & Skin Care Research, LLC 849772207 manufacture