Label: KISS MY FACE SPF-50 DAILY MINERAL SUNSCREEN- zinc oxide cream

  • NDC Code(s): 74154-318-00
  • Packager: WINDMILL HEALTH PRODUCTS LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredient

    Zinc Oxide - 12.00%

    Purpose

    Sunscreen

  • Uses:

    • Helps prevent sunburn
    • Higher SPF gives more sunburn protection
    • If used as directed with other sun protection measures (see ), decreases risk of skin cancer and early skin aging caused by the sun. Directions
  • Warnings:

    not intended for ingestion. 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

    • skin rash or irritation develops and lasts.

    Keep out of reach of children.

    • If swallowed, get medical help or contact Poison Control Center right away..

    If pregnant or breast-feeding,

    • ask a health professional before use.
  • Directions:

    • Apply liberally 15 minute before sun exposure.
    • Reapply:
    • after 80 minutes of swimming or sweating,
    • immediately after towel drying and
    • at least every 2 hours.
    • Children under 6 months: ask a doctor.
    • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use sunscreen with Broad Spectrum SPF 15 or higher and other sun protection measures including: Sun Protection Measures:
    • Limit time in sun, especially from 10am to 2pm.
    • Wear long-sleeved shirts, pants, hats and sunglasses.
  • Inactive Ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbic Acid (Vitamin C), Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Chamomilla Recutita (Chamomile) Extract, Citrullus Lanatus (Watermelon) Extract, Cocos Nucifera (Coconut) Oil, Calendula Officinalis Extract, Camellia Sinensis (Green Tea) Extract, Citric Acid, Decyl Glucoside, Ethylhexylglycerin, Fucus Vesiculosus (Algae) Extract, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Hydroxyethylcellulose, Persea Gratissima (Avocado) Oil, Phenoxyethanol, Polyhydroxystearic Acid, Tagetes Erecta(Lutin) Extract, Tocopheryl Acetate (Vitamin E), Tridecyl Salicylate, Xanthan Gum

  • Other Information

    • Protect this product from excessive heat and direct sun.
  • Questions?

    Call 800-822-4320 or visit www.kissmyface.com

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    KISS MY FACE SPF-50 DAILY MINERAL SUNSCREEN 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74154-318
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION120 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CHAMOMILE (UNII: FGL3685T2X)  
    WATERMELON (UNII: 231473QB6R)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    FUCUS VESICULOSUS (UNII: 535G2ABX9M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74154-318-00118 mL in 1 TUBE; Type 0: Not a Combination Product02/14/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/14/2022
    Labeler - WINDMILL HEALTH PRODUCTS LLC (831136267)
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