Available Formats

• Active Ingredients

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

  
  

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• Purpose

  Sunscreen
  

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• 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.
    

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• 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.

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• 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
    

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• Other Information

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

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• INGREDIENTS AND APPEARANCE

  OCEAN POTION INSTANT DRY 50 DAB-ON SPOTSTICK   avobenzone, homosalate, octisalate, octocrylene liquid

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62802-580 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:62802-580-01 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

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