Label: CVS PHARMACY SPF 30 BEACH GUARD SUN- avobenzone, homosalate, octisalate, octocrylene, oxybenzone 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 November 4, 2022

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

View All Sections
  • Active ingredients

    Avobenzone 2.7%, Homosalate 8.0%, Octisalate 5.0%, Octocrylene 3.5%, Oxybenzone 4.0%

  • 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 with water to remove.

  • ​Stop use and ask a doctor

    if rash occurs.​

  • ​Keep out of reach of 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 with a Broad Spectrum SPF value 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-sleeved shirts, pants, hats, and sunglasses
    • children under 6 months: Ask a doctor

  • Other information

    • protect the product on this container from excessive heat and direct sun
    • may stain or damage some fabrics, materials or surfaces

  • Inactive ingredients

    Water, Dimethicone, Potassium Cetyl Phosphate, Benzyl Alcohol, Butyloctyl Salicylate, Acrylates/C12-22 Alklmethacrylate Copolymer, Caprylyl Glycol, Silica, Cetyl Dimethicone, Beeswax, PPG-12/SMDI Copolymer, Ethylhexylglycerin, Dimethicone/PEG-10/15 Crosspolymer, Trilsiloxane, Ethylhexyl Stearate, Behenyl Alcohol, Sodium Polyacrylate, Trideceth-6, Styrene/Acrylates Copolymer, Disodium EDTA, Glyceryl Stearate, PEG-100 Stearate, Xanthan Gum, Chlorphenesin, Fragrance.

  • Label

    CVS50448A

    CVS30046A

    CVS58842A

  • INGREDIENTS AND APPEARANCE
    CVS PHARMACY   SPF 30 BEACH GUARD SUN
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-146
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE35 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE80 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE27 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYETHYLENE GLYCOL 500 (UNII: 761NX2Q08Y)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)  
    POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-146-27198 mL in 1 BOTTLE; Type 0: Not a Combination Product03/16/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35203/16/2017
    Labeler - CVS Pharmacy (062312574)
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!