Label: SEXY MIX TATTOO ULTRA SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene cream

  • NDC Code(s): 82723-005-01
  • Packager: Aopline Health Industry Technology (Guangzhou) Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 6, 2023

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  • Active Ingredients

    Avobenzone 3%
    Homosalate 5%
    0ctisalate 5%
    0ctocrylene 10%

  • Purpose

    purpose: sunscreen

  • Uses

    Uses
    Helps prevent sunburn
    Higher SPF gives more sunburn protection
    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


    Warnings
    For external use only .
    y 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


    Directions
    Apply liberally 15 minutes before sun exposure
    Reapplly :
    After 80 minutes of swimming or sweating
    Immediately after towel drying
    At least every 2 hours
    Children under 6 months of age : ask a doctor
    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 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-sleeve shirts , pants , hats , and sunglasses .

  • Other Information


    Other information
    protect this product from excessive heat and direct sun

  • Inactive Ingredients


    Inactive ingredients
    Aqua, Propylene Glycol, Glycerin, Inulin Laury
    Carbamate, Vinyl Dimethicone/Methicone
    Silsesquioxane Crosspolymer, Cetearyl Alcohol,
    Potassium Cetyl Phosphate, Sodium Polyacrylate,
    Ethylhexyl Stearate, Trideceth-6, Ammonium
    Acryloyldimethyltaurate/Vp Copolymer,
    Phenoxyethanol, 1, 2-hexanediol
    Hydroxyacetophenone, Maltodextrin, Centella
    Asiatica Leaf Extract Aloe Barbadensis Leaf Water
    Saccharomyces/ice Ferment Filtrate, Butylene
    Glycol, Anhydroxylitol, Tremella Fuciformis
    (Mushroom)Extract, Centella Asiatica Extract, Xylitol

  • Keep out of reach of children.


    Keep out of reach of children . If swallowed , get
    medical help or contact a Poison Control Center right
    away .

  • Stop use


    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 .

  • WHEN USING


    When using this product keep out of eyes , Rinse
    with water to remove
    Stop use and ask a doctor if rash occurs

  • Do not use

    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 .

  • Package Label

    82723-005 TATTOO ULTRA SUNSCREEN

    82723-005

  • INGREDIENTS AND APPEARANCE
    SEXY MIX TATTOO ULTRA SUNSCREEN BROAD SPECTRUM SPF 50 
    avobenzone, homosalate, octisalate, octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82723-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 mg  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 mg  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 mg  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    XYLITOL (UNII: VCQ006KQ1E)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ANHYDROXYLITOL (UNII: 8XWR7NN42F)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CENTELLA ASIATICA LEAF (UNII: 6810070TYD)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82723-005-0190 mL in 1 BOX; Type 0: Not a Combination Product11/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/01/2023
    Labeler - Aopline Health Industry Technology (Guangzhou) Co., Ltd. (715076108)
    Establishment
    NameAddressID/FEIBusiness Operations
    Aopline Health Industry Technology (Guangzhou) Co., Ltd.715076108manufacture(82723-005)
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