Label: KIEHLS ACTIVATED SUN PROTECTOR SUNSCREEN SPF 30 FOR FACE AND BODY FOR ALL SKIN TYPES- ethylhexyl triazone, drometrizole trisiloxane, homosalate, terephthalylidene dicamphor sulfonic acid, ethylhexyl salicylate, bis-ethylhexyloxyphenol methoxyphenyl triazine and diethylamino hydroxybenzoyl hexyl benzoate lotion

  • NDC Code(s): 49967-309-01
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated May 20, 2019

If you are a consumer or patient please visit this version.

  • Directions

    Apply liberally and evenly onto face and/or body prior to sun exposure and massage into skin for complete coverage. Avoid the eye area. Leave ot dry and apply a second time to ensure a generous application. An insufficient amount of product reduces the level of protection. Re-apply frequently to maintain protection, especially after swimming, perspiring, or using a towel. Over-exposure to tht sun is dangerous. Keep babies and young children out of direct sunlight, and well covered. Do not stay too long in the sun, even while using a sunscreen product, because it does not provide you 100% protection. In case of contact with eyes, rinse them immediately and thoroughly.

  • Ingredients

    Ethylhexyl Triazone, Drometrizole Trisiloxane, Homosalate, Terephthalylidene Dicamphor Sulfonic Acid, Ethyhexyl Salicylate, Bis-Ethylhexyloxyphenol methoxyphenyl triazine, Diethylamino hydroxybenzoyl hexyl benzoate

  • Ingredients

    Aqua/Water, Glycerin, C12-15 Alkyl Benzoate, Alcohol Denat., Zea Mays Starch/Corn Starch, Propylene Glycol, Synthetic Wax, Sulfonic Acid, Stearic Acid, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Parfum/Fragrance, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Stearoyl Glutamate, Glycine Soja Oil/Soybean Oil, Tocopherol, Xanthan Gum, Benzyl Salicylate, Benzyl Alcohol, Myristic Acid

  • PRINCIPAL DISPLAY PANEL

    image of tube

  • INGREDIENTS AND APPEARANCE
    KIEHLS ACTIVATED SUN PROTECTOR SUNSCREEN SPF 30 FOR FACE AND BODY FOR ALL SKIN TYPES 
    ethylhexyl triazone, drometrizole trisiloxane, homosalate, terephthalylidene dicamphor sulfonic acid, ethylhexyl salicylate, bis-ethylhexyloxyphenol methoxyphenyl triazine and diethylamino hydroxybenzoyl hexyl benzoate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-309
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4) (ETHYLHEXYL TRIAZONE - UNII:XQN8R9SAK4) ETHYLHEXYL TRIAZONE30 mg  in 1 mL
    DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE50 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
    ECAMSULE (UNII: M94R1PM439) (ECAMSULE - UNII:M94R1PM439) ECAMSULE30 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL40 mg  in 1 mL
    DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ALCOHOL (UNII: 3K9958V90M)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SULFURIC ACID (UNII: O40UQP6WCF)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-309-01150 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    export only01/01/2014
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA, INC.185931458manufacture(49967-309)