KIEHLS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN- drometrizole trisiloxane, octinoxate and ecamsule lotion 
L'Oreal USA Products Inc.

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Drug Facts

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.

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

image of a carton

image of a carton
KIEHLS ULTRA LIGHT DAILY UV DEFENSE SUNSCREEN 
drometrizole trisiloxane, octinoxate and ecamsule lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-258
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DROMETRIZOLE TRISILOXANE (UNII: HC22845I1X) (DROMETRIZOLE TRISILOXANE - UNII:HC22845I1X) DROMETRIZOLE TRISILOXANE40 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE67.5 mg  in 1 mL
ECAMSULE (UNII: M94R1PM439) (ECAMSULE - UNII:M94R1PM439) ECAMSULE120 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-258-011 in 1 CARTON01/01/2022
160 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49967-258-021 in 1 CARTON01/01/2022
230 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:49967-258-031 in 1 CARTON01/01/2022
35 mL in 1 TUBE; Type 0: Not a Combination Product
4NDC:49967-258-041 in 1 CARTON01/01/2022
43 mL in 1 TUBE; Type 0: Not a Combination Product
5NDC:49967-258-051.5 mL in 1 PACKET; Type 0: Not a Combination Product01/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
export only01/01/2022
Labeler - L'Oreal USA Products Inc. (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'OREAL USA, INC.185931458manufacture(49967-258) , pack(49967-258)

Revised: 1/2024
Document Id: f7f39e81-7beb-434d-aaa4-1e54a821013c
Set id: 9eb2fae5-62f7-4bc9-8c5d-43222ab6f365
Version: 2
Effective Time: 20240101
 
L'Oreal USA Products Inc.