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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
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
-
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 gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-455 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Ethylhexyl triazone (UNII: XQN8R9SAK4) (Ethylhexyl triazone - UNII:XQN8R9SAK4) Ethylhexyl triazone 50 mg in 1 mL Diethylamino hydroxybenzoyl hexyl benzoate (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) Diethylamino hydroxybenzoyl hexyl benzoate 30 mg in 1 mL BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL 30 mg in 1 mL DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE 10 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-455-01 1 in 1 CARTON 12/03/2018 07/06/2026 1 60 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-455-02 1 in 1 CARTON 12/03/2018 07/06/2026 2 30 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-455-03 1 in 1 CARTON 12/03/2018 07/06/2026 3 5 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 12/03/2018 07/06/2026 Labeler - L'Oreal USA Products Inc. (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA PRODUCTS, INC. 624244349 manufacture(49967-455)
