KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN UV SERUM BROAD SPECTRUM SPF 50 PLUS SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredients

Avobenzone 3%

Homosalate 7%

Octisalate 5%

Octocrylene 7%

Purpose

Sunscreen

Uses

Warnings

For external use only

Flammble until dry. Do not use near fire, flame or heat.

Do not use

on damaged or broken skin

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

water, glycerin, c15-19 alkane, propanediol, c12-22 alkyl acrylate/hydroxyethylacrylate copolymer, tocopherol, sodium stearoyl glutamate, butylene glycol, cetearyl alcohol, sclerotium gum, hydroxyacetophenone, caprylyl glycol, sodium starch octenylsuccinate, glyceryl stearate, jojoba esters, helianthus annuus (sunflower) seed wax, hydroxypropyl starch phosphate, trisodium ethylenediamine disuccinate, carbomer, sodium lactate, sodium hydroxide, polysorbate 20, polyglycerin-3, palmitoyl tripeptide-1, palmitoyl tetrapeptide-7

image of a carton

image of a carton
KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN UV SERUM BROAD SPECTRUM SPF 50 PLUS SUNSCREEN 
avobenzone, homosalate, octisalate and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-053
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE70 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
C15-19 ALKANE (UNII: CI87N1IM01)  
PROPANEDIOL (UNII: 5965N8W85T)  
TOCOPHEROL (UNII: R0ZB2556P8)  
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
BETASIZOFIRAN (UNII: 2X51AD1X3T)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 64-70) (UNII: 96YYQ5TK1K)  
HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-053-011 in 1 CARTON07/01/2023
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49967-053-021 in 1 CARTON07/01/2023
215 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:49967-053-032 mL in 1 PACKET; Type 0: Not a Combination Product07/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/01/2023
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-053) , pack(49967-053)

Revised: 12/2023
Document Id: a35abbbe-0dfd-4a24-8fb6-98b2367cfcff
Set id: 48980ef3-ebda-450e-9f15-effad27dec9a
Version: 2
Effective Time: 20231230
 
L'Oreal USA Products Inc