Label: KIEHLS ULTRA LIGHT DAILY UV DEFENSE CC SPF 50 ANTI POLLUTION- drometrizole trisiloxane, terephthalylidene dicamphor sulfonic acid, bis-ethylhexyloxyphenol methoxyphenyl triazine, titanium dioxide, ethylhexyl methoxycinnamate and diethylamino hydroxybenzoyl hexyl benzoate cream
- NDC Code(s): 49967-161-01, 49967-161-02, 49967-161-03
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 30, 2023
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Ingredients
Aqua/Water, Butylene Glycol, Glycerin, Dimethicone, Isocetyl Stearate, Alcohol Denate., Propylene Glycol, Stearic Acid, Potassium Cetyl Phosphate, Tocopherol, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Phenoxyethanol, Cetyl alcohol, Cellulose, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Aluminum Hydroxide, Caprylyl Glycol, Sodium Cocoyl Sarcosinate, Carbomer, Scutellaria Baicalensis Extract/Scutellaria Baicalensis Root Extract, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Citric Acid, Isohexadecane, Xanthan Gum, Myristic Acid, Pelargonium Graveolens Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Disodium EDTA, Litchi Chinensis Pericarp Extract, Adenosine, Polysorbate 80, Ethylhexyl Hydroxystearate, Sorbitan Isostearate, Sorbitan Oleate, Polysorbate 60, BHT, Sodium Chloride. May Contain: CI77891/Titanium Dioxide, CI 77491, CI 77492, CI 77499/Iron Oxides, CI 77163/Bismuth Oxychloride
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INGREDIENTS AND APPEARANCE
KIEHLS ULTRA LIGHT DAILY UV DEFENSE CC SPF 50 ANTI POLLUTION
drometrizole trisiloxane, terephthalylidene dicamphor sulfonic acid, bis-ethylhexyloxyphenol methoxyphenyl triazine, titanium dioxide, ethylhexyl methoxycinnamate and diethylamino hydroxybenzoyl hexyl benzoate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-161 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE 40 mg in 1 mL ECAMSULE (UNII: M94R1PM439) (ECAMSULE - UNII:M94R1PM439) ECAMSULE 120 mg in 1 mL BEMOTRIZINOL (UNII: PWZ1720CBH) (BEMOTRIZINOL - UNII:PWZ1720CBH) BEMOTRIZINOL 5 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 40 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 67.5 mg in 1 mL DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ISOCETYL STEARATE (UNII: 3RJ7186O9W) ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) STEARIC ACID (UNII: 4ELV7Z65AP) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) TOCOPHEROL (UNII: R0ZB2556P8) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL ALCOHOL (UNII: 936JST6JCN) POWDERED CELLULOSE (UNII: SMD1X3XO9M) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ISOHEXADECANE (UNII: 918X1OUF1E) XANTHAN GUM (UNII: TTV12P4NEE) MYRISTIC ACID (UNII: 0I3V7S25AW) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) ORANGE OIL (UNII: AKN3KSD11B) EDETATE DISODIUM (UNII: 7FLD91C86K) ADENOSINE (UNII: K72T3FS567) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) POLYSORBATE 60 (UNII: CAL22UVI4M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-161-01 1 in 1 CARTON 01/02/2017 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-161-02 5 mL in 1 TUBE; Type 0: Not a Combination Product 01/02/2017 3 NDC:49967-161-03 3 mL in 1 PACKET; Type 0: Not a Combination Product 01/02/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 01/02/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 185931458 manufacture(49967-161)
