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Bellagio Sunscreen For Face SPF 30 (Lifetech Resources, LLC)

Available Formats

Dosage Form Package Information Links
LOTION 118 mL in 1 TUBE (65643-325-14) Label Information

Complete Bellagio Sunscreen For Face SPF 30 Information

  • SPL UNCLASSIFIED SECTION

    DRUG FACTS


  • ACTIVE INGREDIENTS

    Octinoxate 7.50%, Octocrylene 6.00%, Octisalate 5.00%, Zinc Oxide 2.94%


  • PURPOSE

    Sunscreen


  • USE

    Helps prevent sunburn. Higher SPF gives more sunburn protection.


  • DIRECTIONS FOR USE

    Apply evenly and liberally to all exposed areas before sun exposure. Ensure complete coverage. Reapply as needed or after swimming, towel drying, perspiring, or vigorous activity. Ask a doctor before use on children under 6 months of age.


  • WARNING

    For external use only.

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

    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 right away.


  • INACTIVE INGREDIENTS

    Water, Ethylhexyl Isononanoate, Acrylates Copolymer, Butylene Glycol, Cetyl Alcohol, PEG-100 Stearate, Sorbitan Stearate, Polysorbate-60, Glyceryl Stearate, Dimethicone, Squalane, Hydroxylated Lecithin, Xanthan Gum, Allantoin, Tocopheryl Acetate, Centella Asiatica Extract, Echinacea Angustifolia Extract, Vitis Vinifera (Grape) Seed Extract, Citrus Medica Limonum (Lemon) Peel Extract, Melissa Officinalis Extract, Citric Acid, Triethoxycaprylylsilane, Imidazolidinyl Urea, Sodium Benzoate, Disodium EDTA, Potassium Sorbate.


  • PRINCIPAL DISPLAY PANEL - 118 ML Tube Label

    BELLAGIO®
    SUNSCREEN
    LOTION FOR FACE
    SPF 30

    4 FL OZ / 118 ML

    PRINCIPAL DISPLAY PANEL - 118 ML Tube Label

  • INGREDIENTS AND APPEARANCE
    BELLAGIO SUNSCREEN FOR FACE SPF 30 
    octinoxate, octocrylene, octisalate, and zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65643-325
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 74.25 mg  in 1 mL
    Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 59.4 mg  in 1 mL
    Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 49.5 mg  in 1 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 29.106 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Cetyl Alcohol (UNII: 936JST6JCN)  
    Polyoxyl 100 Stearate (UNII: YD01N1999R)  
    Sorbitan Monostearate (UNII: NVZ4I0H58X)  
    Polysorbate 60 (UNII: CAL22UVI4M)  
    Glyceryl Monostearate (UNII: 230OU9XXE4)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    Squalane (UNII: GW89575KF9)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Allantoin (UNII: 344S277G0Z)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)  
    Lemon Peel (UNII: 72O054U628)  
    MELISSA OFFICINALIS (UNII: YF70189L0N)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Imidurea (UNII: M629807ATL)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Potassium Sorbate (UNII: 1VPU26JZZ4)  
    Product Characteristics
    Color WHITE Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65643-325-14 118 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part352 01/01/2009
    Labeler - Lifetech Resources, LLC (622559110)
    Establishment
    Name Address ID/FEI Business Operations
    Lifetech Resources, LLC 622559110 MANUFACTURE