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EGF UV SHIELD (Dermaesthetics Inc.)

Available Formats

Dosage Form Package Information Links
CREAM 1 TUBE in 1 BOX (58831-1001-2) > 60 g in 1 TUBE (58831-1001-1) Label Information

Complete EGF UV SHIELD Information

  • Drug Fact

    Active ingredient
    Octinoxate 7.50%
    Octisalate 5.00%
    Zinc Oxide 4.90%
    Titanium Dioxide 4.15%
    Amiloxate 2.00%

    Purpose

    Sunscreen

    Keep out of reach of children

    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.

    Indication & usage

    Directions
    Apply generously and evenly 15-20 minutes before sun exposure.

    Use a water resistant sunscreen if swimming or sweating.

    Reapply every 1-2 hours after towel drying, swimming or perspiring.

    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

    Children under 6 months: Ask a doctor

    Warning

    Warnings

    Skin Cancer/Skin Aging Alert:

    Spending time in the sun increases your risk of skin cancer and early skin aging.

    This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

    For external use only.

    Do not use  on damaged or broken skin. If sun irritation develops or increases.

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

    Dosage & administration

    Uses

    Helps prevent sunburn.

    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.

    Inactive ingredient

    Water, Propylene Glycol, Cyclopentasiloxane, Cyclohexasiloxane, Hydrogenated Poly(C6-14 Olefin), Cetyl PEG/PPG-10/1 Dimethicone, PEG-10 Dimethicone, Betaine, Disteardimonium Hectorite, Magnesium Sulfate, Sorbitan Sesquioleate, Aluminum Hydroxide, Stearic Acid, Dimethicone/Vinyl Dimethicone Crosspolymer, Silica, Methyl Methacrylate Crosspolymer, Triethoxycaprylylsilane, Portulaca Oleracea Extract, Poncirus Trifoliata Fruit Extract, Tocopheryl Acetate, Sorbitan Isostearate, Squalane, Simmondsia Chinensis(Jojoba) Seed Oil, Macadamia Ternifolia Seed Oil, Diospyros Kaki Leaf Extract, Cinnamomum Cassia Bark Extract, Artemisia Princeps Leaf Extract, Chrysanthellum Indicum Extract, Chaenomeles Sinensis Fruit Extract, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Juice, Chamomilla Recutita(Matricaria) Flower Extract, Lecithin, Sorbitol, Xanthan Gum, Glyceryl Linoleate, Glyceryl Linolenate, rh-Oligopeptide-1, Acetyl Hexapeptide-8, Sodium Ascorbate, Retinyl Palmitate, Phenoxyethanol, Methylparaben, Propylparaben, Butylparaben, Fragrance


  • EGF UV Shield

    EGF UV Shield

    Net WT. 2.03 fl. oz(60ml)

    image of carton label


  • INGREDIENTS AND APPEARANCE
    EGF UV SHIELD  
    octinoxate cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58831-1001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 g  in 60 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g  in 60 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 4.9 g  in 60 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 4.15 g  in 60 g
    AMILOXATE (UNII: 376KTP06K8) (AMILOXATE - UNII:376KTP06K8) AMILOXATE 2 g  in 60 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    BETAINE (UNII: 3SCV180C9W)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    MAGNESIUM SULFATE (UNII: DE08037SAB)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PURSLANE (UNII: M6S840WXG5)  
    PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    SQUALANE (UNII: GW89575KF9)  
    JOJOBA OIL (UNII: 724GKU717M)  
    MACADAMIA OIL (UNII: 515610SU8C)  
    DIOSPYROS KAKI LEAF (UNII: Q71GF9OBNO)  
    CHINESE CINNAMON (UNII: WS4CQ062KM)  
    ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)  
    CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)  
    CHAENOMELES SINENSIS FRUIT (UNII: 6S5Q1Q537Z)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
    SORBITOL (UNII: 506T60A25R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GLYCERYL MONOLINOLEATE (UNII: 4763AXI84L)  
    GLYCERYL LINOLENATE (UNII: SGB6X4G86K)  
    ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)  
    SODIUM ASCORBATE (UNII: S033EH8359)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    Product Characteristics
    Color white (silver) Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58831-1001-2 1 in 1 BOX
    1 NDC:58831-1001-1 60 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 06/26/2013
    Labeler - Dermaesthetics Inc. (688384549)
    Registrant - Dermaesthetics Inc. (688384549)
    Establishment
    Name Address ID/FEI Business Operations
    Dermaesthetics Inc. 688384549 relabel(58831-1001)
    Establishment
    Name Address ID/FEI Business Operations
    Eyesome Co Ltd 557795360 manufacture(58831-1001)