Label: CVS HEALTH 60 PLUS SENSITIVE SKIN SUN- titanium dioxide, zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 March 24, 2023

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

View All Sections
  • Active ingredients

    Titanium Dioxide 4.9%, Zinc Oxide 4.7%

  • 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

    ALOE BARBADENSIS LEAF JUICE, ALUMINA, ARACHIDYL ALCOHOL, ARACHIDYL GLUCOSIDE, ASCORBIC ACID, BEESWAX, BEHENYL ALCOHOL, BHT, BISABOLOL, BUTYLENE GLYCOL, BUTYLOCTYL SALICYLATE, CAPRYLYL GLYCOL, CASTOR OIL PHOSPHATE, CETYL DIMETHICONE, DIMETHICONE, DIMETHICONE PEG-8 LAURATE, DIPOTASSIUM GLYCYRRHIZATE, DISODIUM EDTA, ETHYLHEXYLGLYCERIN, GLYCERYL STEARATE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, ISOHEXADECANE, METHICONE, METHYLISOTHIAZOLINONE, PANTOTHENIC ACID, PEG-100 STEARATE, PHENOXYETHANOL, PEG-8, POLYAMINOPROPYL BIGUANIDE, POLYMETHYL METHACRYLATE, POLYSORBATE 60, SILICA, STEARIC ACID, STYRENE/ACRYLATES COPOLYMER, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE, TRIMETHYLSILOXYSILICATE, TRISILOXANE, WATER, XANTHAN GUM.

  • Other information

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

  • Label

    CVS29712A1

  • INGREDIENTS AND APPEARANCE
    CVS HEALTH 60 PLUS SENSITIVE SKIN SUN 
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51316-038
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE49 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE47 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496)  
    FARNESOL (UNII: EB41QIU6JL)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
    CETYL DIMETHICONE 150 (UNII: 5L694Y0T22)  
    WATER (UNII: 059QF0KO0R)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    DIMETHICONE PEG-8 LAURATE (UNII: 72MF9C2A18)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    METHICONE (20 CST) (UNII: 6777U11MKT)  
    TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
    POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51316-038-0989 mL in 1 BOTTLE; Type 0: Not a Combination Product11/02/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02011/02/2018
    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!