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Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment

Medically reviewed by Drugs.com. Last updated on Jan 2, 2020.

Dosage form: lotion
Ingredients: SULFUR 100mg in 1mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-895

Drug Facts

Active ingredient


Sulfur 10%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

Do not use on
  • broken skin
  • large areas of the skin

When using this product
  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • apply only to areas with acne

Keep out of reach of children.

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

Directions
  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

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

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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 AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (SULFUR) SULFUR100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
NIACINAMIDE 
GLYCOLIC ACID 
STEARYL ALCOHOL 
GLYCERIN 
PHENOXYETHANOL 
SODIUM HYDROXIDE 
PEG-100 STEARATE 
PHENYLETHYL RESORCINOL 
ALLANTOIN 
ETHYLHEXYLGLYCERIN 
Packaging
#Item CodePackage Description
1NDC:49967-895-011 TUBE in 1 CARTON
120 mL in 1 TUBE
2NDC:49967-895-023 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/01/2016
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIOperations
L'Oreal USA, Inc.185931458manufacture(49967-895)

 
L'Oreal USA Products Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.