Label:
ABSOLUT SKIN SPF 50 MOISTURIZING SUNSCREEN- ethylhexyl methoxycinnamate,ethylhexyl salicylate,methylene bis-benzotriazol...
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  • NDC Code(s): 84066-105-01
  • Packager: Guangzhou Tata Biological Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2025

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  • ACTIVE INGREDIENT
    Ethylhexyl Methoxycinnamate 5% Ethylhexyl Salicylate 3% Methylene Bis-benzotriazolyl tetramethylbutyiphenol 2.5% Octocrylene 2%
  • PURPOSE
    Sunscreen
  • INDICATIONS & USAGE
    Ahigh-performance sunscreen providing broad-spectrum UVA/UVBprotection while hydrating and soothing the skin. This lightweight,non-greasy formula is infused with advanced UV filters, Vitamin E ...
  • WARNINGS
    For external use only.
  • DO NOT USE
    Avoid contact with eyes; rinse thoroughlyif contact occurs.
  • STOP USE
    Stop use to broken orirritated skin
  • OTHER SAFETY INFORMATION
    Protect this product from excessive heat and direct sun. Limiting sunexposure , wearing protective clothing and using sunscreens mayreduce the risk of skin aging, skin cancer and other harmful ...
  • KEEP OUT OF REACH OF CHILDREN
    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
  • INACTIVE INGREDIENT
    Water, Glycerin, Butylene Glycol, lsohexadecane, C12-15 AlkylBenzoate, Propylene Glycol Laurate, PhenylTrimethicone,Polysilicone-15,Diethylamino Hydroxybenzoyl Hexyl Benzoate.Hydrogenated ...
  • DOSAGE & ADMINISTRATION
    Reapplyevery 2 hours when exposed to sunlight.
  • QUESTIONS
    www.myabsolutskin.com
  • PRINCIPAL DISPLAY PANEL
    label
  • INGREDIENTS AND APPEARANCE
    Product Information