Label: PHOTO FINISH FOUNDATION PRIMER SPF 20 cream

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

Drug Label Information

Updated January 3, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS

    Avobenzone 2.00%
    Homosalate 15.00%
    Octisalate 5.00%

  • PURPOSE

    Sunscreen

  • USES

    helps prevent sunburn

  • WARNING

    • 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.
  • DIRECTIONS

    For sunscreen use:

    • apply liberally and evenly 15 minutes before sun exposure
    • apply to all skin exposed to the sun
    • reapply at least every two 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 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
    • children under 6 months of age: ask a doctor
  • INACTIVE INGREDIENTS

    Cyclopentasiloxane, Polysilicone-11, Dimethicone Crosspolymer, C12-15 Alkyl Benzoate, Tocopheryl Acetate, Cola Acuminata (Kola) Seed Extract, Vitis Vinifera (Grape) Seed Extract, Carthamus Tinctorius (Safflower) Seed Oil, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Octyldodecyl Neopentanoate, Tribehenin, Ceramide 2, PEG-10 Rapeseed Sterol, Palmitoyl Oligopeptide, Acetyl Hexapeptide-8, Phenyl Trimethicone, Water\Aqua\Eau, Silica, Laureth-12, Hexyl Laurate, VP/Hexadecene Copolymer, Triethoxycaprylylsilane, Caprylyl Glycol, Hexylene Glycol, Hydrogenated Polydecene, Phenoxyethanol, Potassium Sorbate, Iron Oxides (CI 77491) <ILN39369>

  • OTHER INFORMATION

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

  • INDICATIONS & USAGE

    Stop use and ask a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

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

  • PRINCIPAL DISPLAY PANAL

    PHOTO FINISH PRIMER SPF

  • INGREDIENTS AND APPEARANCE
    PHOTO FINISH FOUNDATION PRIMER SPF 20 
    photo finish foundation primer spf 20 cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59735-450
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    VITIS VINIFERA SEED (UNII: C34U15ICXA)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    CERAMIDE NG (UNII: C04977SRJ5)  
    PEG-10 RAPESEED STEROL (UNII: 258O76T85M)  
    ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LAURETH-12 (UNII: OAH19558U1)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    PALMITOYL HEXAPEPTIDE-12 (UNII: HO4ZT5S86C)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    WATER (UNII: 059QF0KO0R)  
    HEXYL LAURATE (UNII: 4CG9F9W01Q)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COLA ACUMINATA SEED (UNII: 1F8VIW1479)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    TRIBEHENIN (UNII: 8OC9U7TQZ0)  
    Product Characteristics
    ColorpinkScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59735-450-011 in 1 CARTON05/27/2012
    130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/27/2012
    Labeler - MANA PRODUCTS, INC. (078870292)
    Establishment
    NameAddressID/FEIBusiness Operations
    MANA PRODUCTS,INC032870270manufacture(59735-450)
    Establishment
    NameAddressID/FEIBusiness Operations
    MANA PRODUCTS,INC.078870292manufacture(59735-450)