Label: CVS HEALTH AGE DEFENSE SPF 70 FACE- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

  • NDC Code(s): 69842-119-09, 69842-119-10
  • Packager: CVS Pharmacy
  • Category: HUMAN OTC DRUG LABEL

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 11, 2022

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredients

    Avobenzone 3.0%, Homosalate 10.0%, Octisalate 3.0%, Octocrylene 7.0%, Oxybenzone 6.0%

  • 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

  • Inactive ingredients

    water, styrene/acrylates copolymer, polysilicone-15, silica, beeswax, caprylyl methicone, cetyl dimethicone, dimethicone, ethylhexylglycerin, tocopheryl acetate, ascorbic acid, camellia sinensis leaf extract, retinyl palmitate, dipotassium glycyrrhizate, BHT, bisabolol, glyceryl stearate, PEG-100 stearate, sodium polyacrylate, acrylates/C12-22 alkyl methacrylate copolymer, ethylhexyl stearate, xanthan gum, trideceth-6, trimethylsiloxysilicate, disodium EDTA, methylisothiazolinone

  • Other information

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

  • Label

    CVS58801K

    CVS58801A

    CVS30541A

    CVS30541K

  • INGREDIENTS AND APPEARANCE
    CVS HEALTH  AGE DEFENSE SPF 70 FACE
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-119
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    WHITE TEA (UNII: O0M3396E09)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)  
    TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    POLYSILICONE-15 (UNII: F8DRP5BB29)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-119-101 in 1 BOX10/23/2015
    1NDC:69842-119-0989 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35210/23/2015
    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

More Info on this Drug

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