Label: KIEHLS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN- drometrizole trisiloxane, octinoxate and ecamsule lotion
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NDC Code(s):
49967-258-01,
49967-258-02,
49967-258-03,
49967-258-04, view more49967-258-05
- Packager: L'Oreal USA Products Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated January 1, 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.
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Inactive ingredients
water, dimethicone, glycerin, propylene glycol, titanium dioxide, alcohol denat., triethanolamine, stearic acid, potassium cetyl phosphate, nylon-12, palmitic acid, PEG-100 stearate, glyceryl stearate, cetyl alcohol, bis-ethylhexyloxyphenol methoxyphenyl triazine, phenoxyethanol, diethylamino hydroxybenzoyl hexyl benzoate, aluminum hydroxide, methylparaben, sodium cocoyl sarcosinate, caprylyl glycol, carbomer, tocopherol, tromethamine, ethylparaben, acrylamide/sodium acryloyldimethyltaurate copolymer, isohexadecane, xanthan gum, disodium EDTA, adenosine, arginine, polysorbate 80, mannitol, RNA, pyridoxine HCL, disodium adenosine triphosphate, histidine HCL, zea mays extract/corn kernel extract, phenylalanine, faex extract/yeast extract, tyrosine, mentha piperita extract/peppermint leaf extract, rosa gallica extract/rosa gallica flower extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN
drometrizole trisiloxane, octinoxate and ecamsule lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-258 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 OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 67.5 mg in 1 mL ECAMSULE (UNII: M94R1PM439) (ECAMSULE - UNII:M94R1PM439) ECAMSULE 120 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 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) CETYL ALCOHOL (UNII: 936JST6JCN) BEMOTRIZINOL (UNII: PWZ1720CBH) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TOCOPHEROL (UNII: R0ZB2556P8) TROMETHAMINE (UNII: 023C2WHX2V) ETHYLPARABEN (UNII: 14255EXE39) ISOHEXADECANE (UNII: 918X1OUF1E) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ADENOSINE (UNII: K72T3FS567) ARGININE (UNII: 94ZLA3W45F) POLYSORBATE 80 (UNII: 6OZP39ZG8H) MANNITOL (UNII: 3OWL53L36A) PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G) HISTIDINE MONOHYDROCHLORIDE (UNII: 1D5Q932XM6) PHENYLALANINE (UNII: 47E5O17Y3R) YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U) TYROSINE (UNII: 42HK56048U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-258-01 1 in 1 CARTON 01/01/2022 1 60 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-258-02 1 in 1 CARTON 01/01/2022 2 30 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-258-03 1 in 1 CARTON 01/01/2022 3 5 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:49967-258-04 1 in 1 CARTON 01/01/2022 4 3 mL in 1 TUBE; Type 0: Not a Combination Product 5 NDC:49967-258-05 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 01/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date export only 01/01/2022 Labeler - L'Oreal USA Products Inc. (002136794) Establishment Name Address ID/FEI Business Operations L'OREAL USA, INC. 185931458 manufacture(49967-258) , pack(49967-258)
