Label: ULTIMATE SEER SUNSCREEN SPF 55 DAYLOGIC- avobenzone - 3.00% homosalate - 10.00% octisalate - 5.00% octocrylene - 2.75% oxybenzone - 6.00% lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 20, 2018

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

View All Sections
  • Active ingredients                   Purpose

    Avobenzone - 3.00%                Sunscreen
    Homosalate - 10.00%               Sunscreen
    Octisalate - 5.00%                    Sunscreen
    Octocrylene - 2.75%                 Sunscreen
    Oxybenzone - 6.00%                Sunscreen

  • PURPOSE

  • Uses

    • helps prevent sunburn
    • higher SPF gives more sunburn protection

  • WarningsFor external use only

    Do not use on damaged or broken skin
    When using this product keep out of eyes. Rinse with water to remove.
    Stop use and ask a doctor if rash occurs

    Keep out of reach of the children. If product is 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 in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen SPF of 15 or higher and other sun protection measures including:
      - limit time in the sun, especially from 10 a.m. – 2 p.m.
      - wear long sleeve shirts, pants, hats, and sunglasses
    • children under 6 month: Ask a doctor

  • Inactive ingredients

    Behenyl Alcohol, BHT, Butyloctyl Salicylate, Caprylyl Methicone, Dimethicone, Dimethyl Capramide, Disodium EDTA, Ethylhexyl Stearate,
    Ethylhexylglycerin, Ethylparaben, Fragrance, Glyceryl Stearate, Iodopropynyl Butylcarbamate, Methylparaben, PEG-100 Stearate, Phenoxyethanol, Polyester-8, Propylparaben, Silica, Sodium Polyacrylate, Styrene/Acrylates Copolymer, Trideceth-6, Trimethylsiloxysilicate, VP/Hexadecene Copolymer, Water, Xanthan Gum

  • Other information

    • protect this product from excessive heat and direct sun • may stain fabrics

  • Questions? 1-800-RITEAID (1-800-748-3243)

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    ULTIMATE SEER SUNSCREEN SPF 55  DAYLOGIC
    avobenzone - 3.00% homosalate - 10.00% octisalate - 5.00% octocrylene - 2.75% oxybenzone - 6.00% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-1241
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Avobenzone (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) Avobenzone3 g  in 100 mL
    Homosalate (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) Homosalate10 g  in 100 mL
    Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) Octisalate5 g  in 100 mL
    Octocrylene (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) Octocrylene2.75 g  in 100 mL
    Oxybenzone (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) Oxybenzone6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DOCOSANOL (UNII: 9G1OE216XY)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Butyloctyl Salicylate (UNII: 2EH13UN8D3)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    Dimethyl Capramide (UNII: O29Y6X2JEZ)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Ethylhexyl Stearate (UNII: EG3PA2K3K5)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    Ethylparaben (UNII: 14255EXE39)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)  
    Methylparaben (UNII: A2I8C7HI9T)  
    PEG-100 Stearate (UNII: YD01N1999R)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)  
    Propylparaben (UNII: Z8IX2SC1OH)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Trideceth-6 (UNII: 3T5PCR2H0C)  
    VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
    WATER (UNII: 059QF0KO0R)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-1241-389 mL in 1 TUBE; Type 0: Not a Combination Product06/30/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35206/30/2016
    Labeler - Rite Aid (014578892)
    Registrant - Product Quest Mfg (927768135)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg927768135manufacture(11822-1241) , label(11822-1241)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!