Label: BEAUTY HYDRATING- homosalate, zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 29, 2024

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  • Active ingredients

    Homosalate 5.0%

    Zinc oxide 3.0%

  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • if used as directed with other sun protection measures (see Directions), decreases the rise 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 swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply liberally 15 minutes before sun exposure
    • apply to all skim exposed to the sun
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming or sweating
    • 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 highter and other sun protection measures including:
    • limit the time in the sun, especially from 10 a.m. - 2 p.m.
    • wear long-sleeved shirts, pants, hats and sunglasses
    • children under 6 months of age: ask a doctor
  • Other information

    • protect the product from excessive heat and direct sun
  • Inactive ingredients

    water, glycerin, isohexadecane, sodium acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, laureth-7, cyclopentasiloxane, cyclohexasiloxane, tocopheryl acetate, Aloe barbadensis leaf extract, steareth-21, stearyl alcohol, caprylyl glycol, behenyl alcohol, phenoxyethanol, cetyl alcohol, fragrance, hydroxyacetophenone, disodium EDTA, steareth-2, oleth-3 phosphate

  • Disclaimer

    *This product is not manufactured or distributed by Procter & Gamble, distributor of Olay ® Complete UC365 Daily Moisturizer with Sunscreen Broad Spectrum SPF 15 Normal.

    May stain or damage some fabrics or surfaces.

  • Adverse Reactions

    DISTRIBUTED BY TOPCO ASSOCIATES LLC

    ITASCA, IL 60143 © TOPCO VIJA0724

    QUESTIONS? 1-888-423-0139

    topcare@topco.com 

    www.topcarebrand.com

    Scan here for more information or call 1-888-423-0139

  • principal display panel - side panels

    Top Care ® beauty

    ALL-DAY MOISTURIZER

    Sunscreen Lotion

    ALL-DAY MOISTURE

    Formulated with Vitamin E and nourishing beauty moisture that absorbs quickly into skin and lasts all day to help your skin stay soft, smooth and beautiful.

    UV PROTECTION

    Broad-spetrum UVA and UVB protection with SPF 15to help prevent premature skin damage

    QUALITY GUARANTEED

    This TopCare ® product is laboratory tested to guarantee its highest quality. Your total satisfaction is guaranteed.

    Top Care ® beauty

    ALL-DAY MOISTURIZER

    Sunscreen Lotion

    Light, non-greasy formula

    Non-comedogenic (won't clog pores)

    Phthalate free

    Light, fast absorbing moisture lasts all day

    Softens and smoothes for radiant-looking skin

  • principal display panel

    Top Care ® beauty

    ALL-DAY MOISTURIZER

    Sunscreen Lotion

    For Normal Skin

    Compare to OLAY ® *

    Broad spectrum SPF 15

    Dermatologist tested

    SPF 15

    6 FL OZ (177mL)

    image description

  • INGREDIENTS AND APPEARANCE
    BEAUTY HYDRATING 
    homosalate, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-513
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    LAURETH-7 (UNII: Z95S6G8201)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    STEARETH-2 (UNII: V56DFE46J5)  
    OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-513-301 in 1 PACKAGE06/02/2020
    1177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/02/2020
    Labeler - Topco (006935977)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(36800-513)
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