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mark. For Gooness Face (Avon Products, Inc.)

Available Formats

Dosage Form Package Information Links
LOTION 1 JAR in 1 CARTON (10096-0144-2) > 50 mL in 1 JAR (10096-0144-1) Label Information

Complete mark. For Gooness Face Information

  • ACTIVE INGREDIENT

    ​Active Ingredients

    ​​Homosalate 8.0%.........

    Octinoxate 7.5%...........

    Octisalate 5.0%............

    Oxybenzone 5.0%..........

    Avobenzone 3.0%..........

    ​ Purpose

    ​ ​...........Sunscreen

    ...........Sunscreen

    ...........Sunscreen

    ...........Sunscreen

    ...........Sunscreen


  • INDICATIONS & USAGE

    ​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


  • WARNINGS

    ​Warnings

    ​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.

    ​Stop use and ask a doctor if ​rash occurs

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


  • DOSAGE & ADMINISTRATION

    ​Directions

    • ​​apply liberally 15 minutes before sun exposure
    • children under 6 months of age: ask a doctor
    • reapply at least every 2 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 SPF 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


  • STORAGE AND HANDLING

    ​Other information

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


  • INACTIVE INGREDIENT

    ​Inactive Ingredients:​ ​ Water/Eau, Butylene Glycol, Glycerin, PEG-8, Dimethicone, Nylon-12, Citrus Medica Limonum (Lemon) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Fumaria Officinalis Flower/Leaf/Stem Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Vanilla Planifolia Fruit Extract, Theobroma Cacao (Cocoa) Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Vitis Vinifera (Grape) Fruit Extract, Tromethamine, Silica, Trimethylsiloxysilicate, Glyceryl Stearate, Hydrogenated Lecithin, Carbomer, Polyglyceryl-3 Diisostearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Squalane, Dimethicone/Vinyl Dimethicone Crosspolymer, Caprylic/Capric Triglyceride, Fumaric Acid, Citric Acid, Disodium EDTA, Benzyl Alcohol, Cetyl Alcohol, Polysorbate 60, Methylparaben, Propylparaben


  • QUESTIONS

    ​Questions or Comments? ​ ​Call toll free ​1-800-meetmark


  • INGREDIENTS AND APPEARANCE
    MARK. FOR GOONESS FACE  ANTIOXIDANT SKIN MOISTURIZING
    homosalate, octinoxate, octisalate, oxybenzone, avobenzone lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0144
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 50 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg  in 1 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10096-0144-2 1 in 1 CARTON
    1 NDC:10096-0144-1 50 mL in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 03/08/2013
    Labeler - Avon Products, Inc. (001468693)
    Establishment
    Name Address ID/FEI Business Operations
    Avon Products, Inc. 005149471 manufacture(10096-0144)