Label: KIEHLS ULTRA LIGHT DAILY UV DEFENSE AQUA GEL SPF 50 ANTI-POLLUTION- ethylhexyl triazone, diethylamino hydroxybenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and drometrizole trisiloxane gel

  • NDC Code(s): 49967-455-01, 49967-455-02, 49967-455-03
  • Packager: L'Oreal USA Products Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated January 30, 2024

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  • Directions

    Apply in the morning at the end of your daily skincare routine. Avoid eye area. In case of contact with eyes, rinse immediately and thoroughly. 

    Over-exposure to the sun in dangerous. Keep babies and young children out of direct sunlight. Do not stay too long in the sun, even while using a sunscreen product because it does not provide you 100% protection. Apply the sunscreen product just before sun exposure. Re-apply frequently and generously to maintain protection, especially after swimming, perspiring or toweling.

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    KIEHLS ULTRA LIGHT DAILY UV DEFENSE AQUA GEL SPF 50 ANTI-POLLUTION 
    ethylhexyl triazone, diethylamino hydroxybenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine and drometrizole trisiloxane gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-455
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Ethylhexyl triazone (UNII: XQN8R9SAK4) (Ethylhexyl triazone - UNII:XQN8R9SAK4) Ethylhexyl triazone50 mg  in 1 mL
    Diethylamino hydroxybenzoyl hexyl benzoate (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) Diethylamino hydroxybenzoyl hexyl benzoate30 mg  in 1 mL
    BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL30 mg  in 1 mL
    DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE10 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    CETETH-10 (UNII: LF9X1PN3XJ)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ADENOSINE (UNII: K72T3FS567)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    GENTIANA LUTEA ROOT (UNII: S72O3284MS)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    MENTHA PIPERITA (UNII: 79M2M2UDA9)  
    SHEANUT (UNII: 84H6HBP32L)  
    ROSA GALLICA FLOWER (UNII: X8W61WUV70)  
    SORBITOL (UNII: 506T60A25R)  
    MORINGA OLEIFERA SEED (UNII: TIX5482832)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-455-011 in 1 CARTON12/03/201807/06/2026
    160 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:49967-455-021 in 1 CARTON12/03/201807/06/2026
    230 mL in 1 TUBE; Type 0: Not a Combination Product
    3NDC:49967-455-031 in 1 CARTON12/03/201807/06/2026
    35 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    export only12/03/201807/06/2026
    Labeler - L'Oreal USA Products Inc. (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA PRODUCTS, INC.624244349manufacture(49967-455)