FACE FACTOR (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) LOTION [KISS MY FACE, LLC]

FACE FACTOR (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) LOTION [KISS MY FACE, LLC]
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NDC 65364-219-01
Set ID 7d7f7750-c038-4607-920d-1869cf7d837e
Category HUMAN OTC DRUG LABEL
Packager Kiss My Face, LLC
Generic Name
Product Class
Product Number
Application Number PART352
  • Active ingredients

    Avobenzone (3.0%), Homosalate (6.0%), Octinoxate (7.5%), Octisalate (5.0%), Titanium Dioxide (3.0%).

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  • Inactive ingredients

    Acetyl Hexapeptide-8, Acrylates Copolymer, Aloe Barbadensis Leaf Juice, a-Lipoic Acid, Aqua, Ascorbyl Palmitate, Camellia Sinensis (Green Tea) Extract, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Cucumis Sativus (Cucumber) Extract, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate SE, Glycrrhiza Glabra (Licorice) Extract, Helianthus Annuus (Sunflower) Oil, Lavandula Angustifolia (Lavender) Oil, Lecithin, Phenoxyethanol, Polysorbate-20, Potassium Hydroxide, Saccharide Isomerate, Sodium Hyaluronate, Sorbitan Olivate, Stearyl Alcohol, Styrene/Acrylate Copolymer, Zemea Propanediol.

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  • Keep out of reach of children

    Keep out of reach of children.

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  • Directions

    Apply liberally 15 minutes before sun exposure

    Reapply ater 40 minutes swimming/sweating, immediately after towel drying, and at least every 2 hours

    Children under 6 months ask a doctor

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  • Use

    Helps prevent sunburn

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  • Purpose

    sunscreen

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  • Warnings

    For external use only

    Do not use on damaged or broken skin

    Stop use and ask doctor if rash occurs

    When using this product keep out of eyes. Rinse with water to remove.

    If swallowed get medical help or contact a poison control center right away

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  • Package display
  • INGREDIENTS AND APPEARANCE
    FACE FACTOR 
    avobenzone, homosalate, octinoxate, octisalate, titanium dioxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65364-219
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 6 g  in 100 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g  in 100 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 3 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)  
    DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)  
    .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)  
    WATER (UNII: 059QF0KO0R)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    CUCUMIS SATIVUS LEAF (UNII: Q6S42514LP)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LICORICE (UNII: 61ZBX54883)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65364-219-01 100 g in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part352 01/01/2015
    Labeler - Kiss My Face, LLC (041794279)
    Registrant - Kiss My Face, LLC (041794279)
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