| NDC | 49967-449-01, 49967-449-02, 49967-449-03, 49967-449-04 |
| Set ID | 3c374e58-e897-495a-b005-0231391c5e94 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | L'Oreal USA Products Inc |
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| Product Class | |
| Product Number | |
| Application Number |
- Ingredients
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Ingredients
Aqua/Water, Glycerin, Propylene Glycol, Alcohol Denat., Triethanolamine, Stearic Acid, Potassium Cetyl Phosphate, Nylon-12, Palmitic Acid, PEG-100 Stearate, Glyceryl Stearate, Phenoxyethanol, Cetyl Alcohol, Cellulose, Citric Acid, Aluminum Hydroxide, Caprylyl Glycol, Sodium Cocoyl Sarcosinate, Carbomer, Tocopherol, Tromethanime, Scutellaria Baicalensis Extract/Scutellaria Baicalensis Root Extract, Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Isohexadecane, Xanthan Gum, Myristic Acid, Disodium EDTA, Adenosine, Polysorbate 80, Arginine, Mannitol, Disodium Adenosine Triphosphate, RNA, Pyridoxane HCL, Sorbitan Oleate, Sorbitol, Pentylene Glycol, BHT, Histidine HCL, Zea Mays Kernel Extract/Corn Kernel Extract, Sodium Chloride, Faex Extract/Yeast Extract, Phenylalanine, Mentha Piperita Extract/Perppermint Extract, Rosa Gallica Flower Extract, Tyrosine, Sorbic Acid
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS DERMATOLOGIST SOLUTIONS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN SPF 50 HIGH PROTECTION ANTI-POLLUTION LIGHTWEIGHT FORMULA FOR ALL SKIN TYPES
drometrizole trisiloxane, titanium dioxide, ecamsule, bemotrizinol, diethylamino hydroxybenzoyl hexyl benzoate and octinoxate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-449 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 TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 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 DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE - UNII:ANQ870JD20) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 5 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 67.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) TROLAMINE (UNII: 9O3K93S3TK) STEARIC ACID (UNII: 4ELV7Z65AP) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) NYLON-12 (UNII: 446U8J075B) PALMITIC ACID (UNII: 2V16EO95H1) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL ALCOHOL (UNII: 936JST6JCN) POWDERED CELLULOSE (UNII: SMD1X3XO9M) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) TOCOPHEROL (UNII: R0ZB2556P8) TROMETHAMINE (UNII: 023C2WHX2V) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) ISOHEXADECANE (UNII: 918X1OUF1E) XANTHAN GUM (UNII: TTV12P4NEE) MYRISTIC ACID (UNII: 0I3V7S25AW) EDETATE DISODIUM (UNII: 7FLD91C86K) ADENOSINE (UNII: K72T3FS567) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ARGININE (UNII: 94ZLA3W45F) MANNITOL (UNII: 3OWL53L36A) ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) sorbitol (UNII: 506T60A25R) PENTYLENE GLYCOL (UNII: 50C1307PZG) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) HISTIDINE MONOHYDROCHLORIDE (UNII: 1D5Q932XM6) CORN (UNII: 0N8672707O) SODIUM CHLORIDE (UNII: 451W47IQ8X) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) PHENYLALANINE (UNII: 47E5O17Y3R) mentha piperita (UNII: 79M2M2UDA9) ROSA GALLICA FLOWER (UNII: X8W61WUV70) TYROSINE (UNII: 42HK56048U) SORBIC ACID (UNII: X045WJ989B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-449-01 1 in 1 CARTON 12/01/2017 1 60 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-449-02 1 in 1 CARTON 12/01/2017 2 30 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-449-03 5 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2017 4 NDC:49967-449-04 3 mL in 1 PACKET; Type 0: Not a Combination Product 12/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 12/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 185931458 manufacture(49967-449)
