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UltrasolSunscreen (Fischer Pharmaceuticals Ltd)

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LOTION 250 g in 1 BOTTLE, PLASTIC (59886-308-55) Label Information

Complete UltrasolSunscreen Information

  • PRINCIPAL DISPLAY PANEL

    PDP and Back

    Dr. Fischer Ultrasol

    KIDS Sunscreen Lotion

    SPF34

    Broad Spectrum

    UVA and UVB Protection

    Pediatrician Recommended

    SCIENCE INSIDETM - SUPERIOR SUN TECHNOLOGY

    250 ML. 8.45 FL.OZ.

    FISCHER PHARMACEUTICALS

    (Back of Package):

    Manufactured by:

    Fischer Pharmaceuticals Ltd.

    Bnei Brak, Israel, 51553

    Made in Israel

    www.dr-fischer.com

    NO ANIMAL INGREDIENTS - NO ANIMAL TESTING

    24m

    Dr. Fischer - Tried and Tested



  • Drug Facts

    Active Ingredients                                                                                             Purpose
    Avobenzone 2.0%, Octinoxate 7.5%, Octisalate 3.0%, Oxybenzone 3.0% ....... Sunscreen


  • Uses

    helps prevent sunburn higher SPF gives more sunburn protection
    helps protect the skin against the harmful effects of UVA and UVB rays
    retains SPF after 80 minutes of activity in the water or sweating


  • Warnings

    For external use only

    When using this product

    avoid contact with the eyes. If contact occurs rinse
    thoroughly with water

    Stop use and ask a doctor if

    rash or irritation develops and lasts.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison
    Control Center immediately.


  • Directions

    apply generously and evenly to all exposed areas before sun exposure
    reapply as needed or after towel drying, swimming, perspiring or vigorous activity
    children under 6 months of age: ask a doctor


  • Other Information

    may stain some fabrics
    Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens
    may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.


  • Inactive Ingredients

    Acrylates / C10-30 Alkyl Acrylate Crosspolymer,
    Butylparaben, Chlorophenesin, Disodium EDTA, Ethylparaben, Fragrance, Glyceryl
    Stearate, Green Tea (Camellia Sinensis) Leaf Extract, Iodopropynyl Butylcarbamate,
    Isopropyl Myristate, Methylparaben, Phenoxyethanol, Polyethylene, Potassium Cetyl
    Phosphate, Propylene Glycol, Propylparaben, Sodium Hydroxide, Stearic Acid, Stearyl
    Alcohol, Tocopheryl Acetate, Water.


  • Questions or Comments?

    Call 1-877-212-1985 Mon-Fri


  • INGREDIENTS AND APPEARANCE
    ULTRASOLSUNSCREEN  KIDS SUNSCREEN LOTION SPF 34
    avobenzone, octinoxate, octisalate, oxybenzone lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:59886-308
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone 2 g  in 100 g
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 7.5 g  in 100 g
    Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 3 g  in 100 g
    Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone 3 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    Butylparaben (UNII: 3QPI1U3FV8)  
    Chlorphenesin (UNII: I670DAL4SZ)  
    Ethylparaben (UNII: 14255EXE39)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Propylparaben (UNII: Z8IX2SC1OH)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Stearyl Alcohol (UNII: 2KR89I4H1Y)  
    Water (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59886-308-55 250 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 04/01/2010
    Labeler - Fischer Pharmaceuticals Ltd (600158976)
    Establishment
    Name Address ID/FEI Business Operations
    Fischer Pharmaceuticals Ltd 600158976 manufacture