Label: VITAMIN E VITALIZING SUNSCREEN cream

  • NDC Code(s): 83872-270-01
  • Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 3, 2024

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  • ACTIVE INGREDIENT

    Octinoxate
    Octocrylene
    Zinc Oxide

  • PURPOSE

    sunburn protection

  • INDICATIONS

    sunburn protection

  • Warnings

    For external use only.

  • Do not use

  • When using this product

    Wnen using tnis product keep out of eyes. Rinse with water to remove.

  • Stop use and ask a doctor

    Stop use and ask a doctor if rash occurs

  • Keep out of reach of children.

    Keep out of reach of children.

  • Directions for use

    apply liberally 15 minutes before sun exposure,reapply at least every 2 hours.use a water resistant sunscreen if swimming or sweating.Sun Protection Measures: $pending time in the sunincreases your risk of skin cancer and early skin aging.To decrease this risk, reqularly use a sunscreen with a B roadSpectrum SPF value of 15 or higher and other sun protectionmeasures including :limit time in the sun, especially from 10 a.m. - 2 p.m.and wear longsleeved shirts, pants, hats, and sunglasses.

  • INACTIVE INGREDIENT

    Water,
    Glycerin,
    Cetearyl Alcohol,
    Butylene Glycol,
    Niacinamide,
    Sodium Hyaluronate,
    Tocopherol,
    Centella Asiatica Extract,
    Camellia Sinensis Leaf Extract, Ethylhexylglycerin, CarbomerTriethaxycaprylylsilane, Phenoxyethanol,
    Xanthan Gum, AdditionalIngredients (Fragrances, Stabilizers, etc,), Dibutyl Adipate,
    Polymethylsilsesquioxane,
    Coco-Caprylate'Caprate, Hyaluronic Acid.

  • Other Information

    Store in a cool, dry place. "Avoid direct sunlight.
    Consult a dermatologist if you have any questions.

  • label

    label

  • INGREDIENTS AND APPEARANCE
    VITAMIN E VITALIZING SUNSCREEN 
    vitamin e vitalizing sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-270
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE100 g  in 1 mg
    Inactive Ingredients
    Ingredient NameStrength
    AVOCADO FRUIT WATER (UNII: QY52B5ZP10) 100 g  in 1 mg
    OCTINOXATE (UNII: 4Y5P7MUD51) 100 g  in 1 mg
    .ALPHA.-TOCOPHEROL CALCIUM SUCCINATE, D- (UNII: BVK87L5TNB) 100 g  in 1 mg
    PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A) 100 g  in 1 mg
    OCTOCRYLENE (UNII: 5A68WGF6WM) 100 g  in 1 mg
    CETEARYL BEHENATE (UNII: 7ARI9LTH0U) 100 g  in 1 mg
    ISONIACINAMIDE (UNII: 4H3BH6YX9Q) 100 g  in 1 mg
    1-BUTYLGLYCERIN (UNII: 8834DFG5HH) 100 g  in 1 mg
    1,3-BUTYLENE GLYCOL 1-PROPIONATE (UNII: 17U77WTV66) 100 g  in 1 mg
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-270-0150 mg in 1 BOTTLE; Type 0: Not a Combination Product07/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/03/2024
    Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen XiaoMai Manufacturing Co., Ltd.712999147manufacture(83872-270)
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