KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL TARGETED ACNE SPOT TREATMENT- sulfur lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient


Sulfur 10%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

Do not use on

When using this product

Keep out of reach of children.

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

Directions

Inactive ingredient

water, niacinamide, zea mays (corn) starch, glycolic acid, stearyl alcohol, glycerin, octyldodecyl myristate, cetearyl alcohol, glyceryl stearate, magnesium aluminum silicate, phenoxyethanol, polyacrylamide, ceteareth-20, sodium hydroxide, PEG-100 stearate, phenylethyl resorcinol, tocopheryl acetate, C13-14 isoparaffin, disodium EDTA, laureth-7, allantoin, aloe barbadensis leaf juice, hydrogenated lecithin, ethylhexylglycerin, glycyrrhiza glabra (licorice) root extract

Questions or comments?

Call toll free 1-800-946-4453

image of a carton

image of a carton
KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL TARGETED ACNE SPOT TREATMENT 
sulfur lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-895
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
NIACINAMIDE (UNII: 25X51I8RD4)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PHENYLETHYL RESORCINOL (UNII: G37UFG162O)  
ALLANTOIN (UNII: 344S277G0Z)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-895-011 in 1 CARTON11/01/2016
120 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49967-895-023 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
3NDC:49967-895-031.5 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
4NDC:49967-895-043 mL in 1 TUBE; Type 0: Not a Combination Product11/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00611/01/2016
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458analysis(49967-895)
Establishment
NameAddressID/FEIBusiness Operations
Englewood Lab, Inc.172198223manufacture(49967-895) , pack(49967-895)

Revised: 12/2023
Document Id: 1cb9aca2-b493-4ee2-85c9-0001329654fc
Set id: 217c697e-0260-46d5-a202-ce7345eadd94
Version: 12
Effective Time: 20231230
 
L'Oreal USA Products Inc