KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene cream 
L’Oreal USA Products Inc

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Drug Facts

Active ingredient

Avobenzone 3%

Homosalate 5%

Octisalate 5%

Octocrylene 7%

Purpose

Sunscreen

Uses

Warnings

For external use only

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

For sunscreen use:

     ● limit time in the sun, especially from 10 a.m. – 2 p.m.

     ● wear long-sleeved shirts, pants, hats, and sunglasses

Other information

protect the product in this container from excessive heat and direct sun

Inactive ingredients

water, glycerin, dimethicone, glyceryl stearate, hydroxypropyl tetrahydropyrantriol, silica, PEG-100 stearate, propylene glycol, euphorbia cerifera (candelilla) wax, phenoxyethanol, ammonium polyacryloyldimethyl taurate, stearic acid, dicaprylyl carbonate, cetyl alcohol, palmitic acid, capryloyl salicylic acid, caprylyl glycol, xanthan gum, dimethicone/vinyl dimethicone crosspolymer, fragrance, disodium EDTA, tocopherol, sodium hyaluronate, adenosine, linalool, sodium hydroxide, jasminum officinale (jasmine) flower extract, citronellol, geraniol, citral, benzyl alcohol, citric acid

Questions or comments?

Call toll free 1-800-946-4453

Monday - Friday (9 a.m. to 5 p.m. EST)

image of a label

image of a label
KIEHLS SINCE 1851 SUPER MULTI CORRECTIVE BROAD SPECTRUM SPF 30 SUNSCREEN 
avobenzone, homosalate, octisalate and octocrylene cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-410
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) HOMOSALATE50 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)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HYDROXYPROPYL TETRAHYDROPYRANTRIOL (UNII: 4U3GMG1OT1)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CANDELILLA WAX (UNII: WL0328HX19)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PALMITIC ACID (UNII: 2V16EO95H1)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
XANTHAN GUM (UNII: TTV12P4NEE)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
TOCOPHEROL (UNII: R0ZB2556P8)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
ADENOSINE (UNII: K72T3FS567)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)  
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)  
GERANIOL (UNII: L837108USY)  
CITRAL (UNII: T7EU0O9VPP)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-410-0150 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
2NDC:49967-410-02125 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
3NDC:49967-410-0375 mL in 1 JAR; Type 0: Not a Combination Product07/01/2015
4NDC:49967-410-043 mL in 1 PACKET; Type 0: Not a Combination Product07/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/01/2015
Labeler - L’Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L’Oreal USA, Inc.185931458manufacture(49967-410)

Revised: 1/2024
Document Id: fce707d4-51c3-486f-82fa-eb80d11498f6
Set id: 733e7853-ab11-4887-83a2-b9d95c163453
Version: 6
Effective Time: 20240101
 
L’Oreal USA Products Inc