Label: FACE SPF 47 SETTING- face spf 47 setting spray spray

  • NDC Code(s): 82723-001-01
  • Packager: Aopline Health Industry Technology (Guangzhou) Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active Ingredients

    Homosalate 8.0%

    Octisalate 5.0%

    Octocrylene 3.0%

    Avobenzone 3.0%

  • Purpose

    Sunscreen

  • Uses

    Helps prevent sunburn. If used as directed with other sun protection measures, decrease the risk of skin cancer and early skin aging caused by sun.

  • Warnings

    For External Use Only.

    Do not use on damaged or broken skin.

    Keep out of reach of children.

    Keep out of eyes. Rinse with water to remove.

    Stop use and ask a physician if rash occurs.

    Keep out of reach of children . If product is swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    •Apply to face 15 minutes before sun exposure.

    Reapply every 2 hours.

  • Other Information

    Children under 6 months ask a physician.

  • Inactive Ingredients

    Vitamin E, Vitamin C, Hyaluronic Acid, Niacinamide, Peppermint Extract, Eucalyptus Extract, Sunflower Seed Oil, Tea Tree Extract, Alcohol, Cyclohexasiloxane, Cyclopentasiloxane, Ethylhexyl Palmitate

  • Keep out of reach of children.

    Keep out of reach of children.

  • Stop use

    Stop use and ask a physician if rash occurs.

  • WHEN USING

    For External Use Only.

    Do not use on damaged or broken skin.

    Keep out of reach of children.

    Keep out of eyes. Rinse with water to remove.

    Stop use and ask a physician if rash occurs.

    Keep out of reach of children . If product is swallowed, get medical help or contact a Poison Control Center immediately.

  • Do not use

    Do not use on damaged or broken skin.

  • Package Label

    82723-001-01 50mL

  • INGREDIENTS AND APPEARANCE
    FACE SPF 47 SETTING 
    face spf 47 setting spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82723-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE3 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE8 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ALCOHOL (UNII: 3K9958V90M)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    PEPPERMINT (UNII: V95R5KMY2B)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82723-001-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/07/2022
    Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aopline Health Industry Technology (Guangzhou) Co., Ltd.715076108manufacture(82723-001)
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