Label: SUNSCREEN- avobenzone, homosalate, octisalat, octocrylene lotion

  • NDC Code(s): 72476-117-21
  • Packager: Retail Business Services, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 6, 2024

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  • Active ingredient

    Avobenzone 
    Homosalate 
    Octisalate
    Octocrylene

    Purpose

    sunscreen

  • Uses

    • helps prevent sunburn
    • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer
  • Warnings

    For external use only

    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 skin exposed to the sun
    • reapply: after 80 minute of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
    • Sun Protection Measures. Spending time in the sun increases your rist of skin cancer and early skin aging.  To decrease this risk, regularly use a sunscreen with 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
    • childre under 6 months of age: ask a doctor
  • Other information

    protect the product in this container from excessive heat and dirtect sun

  • Inactive ingredients

    water, diethylhexyl 2,6-naphthalate, styrene/acrylates copolymer, silica, glyceryl stearate, PEG-100 stearate, beeswax, cyclopentasiloxane, acrylates/dimethicone copolymer, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, chlorphenesin, benzyl alcohol, triethanolamine, disodium EDTA, BHT

  • ADVERSE REACTIONS

    May stain or damage some fabrics or surfaces

    This product is not manufactured or distributed by Johnson & Johnson Consumer, Inc., distributor of  Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 100+

    DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC

    SALISBURY, NC 28147

    1-833-992-3872

    Quality guaranteed or your money back.

  • principal display panel

    CAREONE

    Compare to Neutrogena Ultra Sheer Sunscreen Broad Spectrum SPF 100+

    SHEET TOUCH

    Sunscreen Lotion

    SPF 100

    UVA/UVB PROTECTION

    Broad Spectrum SPF 100

    • Water resistant (80 min)
    • Clean and lightweight feel
    • Quickly absorbs
    • Oxybenzone & Octinoxate Free Formula

    NET 3 FL OZ (88 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    SUNSCREEN 
    avobenzone, homosalate, octisalat, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72476-117
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE90 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE2250 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE250 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1000 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72476-117-2188 mL in 1 TUBE; Type 0: Not a Combination Product11/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/30/2021
    Labeler - Retail Business Services, LLC (967989935)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(72476-117)
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