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Kiehls Since 1851 Dermatologist Solutions Breakout Control Acne Treatment Facial

Dosage form: lotion
Ingredients: SALICYLIC ACID 15mg in 1mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-875

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredient

Salicylic acid 1.5%

Purpose

Acne treatment

Uses
  • for the treatment of acne
  • helps prevent new acne blemishes

Warnings

For external use only

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.

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 ingredients

water, aloe barbadensis leaf juice, di-C12-13 alkyl malate, niacinamide, cyclohexasiloxane, propylene glycol, aluminum starch octenylsuccinate, PEG-100 stearate, glyceryl stearate, cetyl alcohol, acrylates/C10-30 alkyl acrylate crosspolymer, sodium hydroxide, capryloyl salicylic acid, xanthan gum, zinc PCA, zingiber officinale (ginger) root extract, stearyl alcohol, myristyl alcohol, citric acid, potassium sorbate, octadecenedioic acid, sodium benzoate, citral, BHT

Questions or comments?

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KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL ACNE TREATMENT FACIAL 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-875
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID15 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
NIACINAMIDE 
PROPYLENE GLYCOL 
ALUMINUM STARCH OCTENYLSUCCINATE 
PEG-100 STEARATE 
CETYL ALCOHOL 
SODIUM HYDROXIDE 
CAPRYLOYL SALICYLIC ACID 
XANTHAN GUM 
STEARYL ALCOHOL 
MYRISTYL ALCOHOL 
OCTADECENEDIOIC ACID 
CITRAL 
Packaging
#Item CodePackage Description
1NDC:49967-875-011 BOTTLE in 1 CARTON
160 mL in 1 BOTTLE
2NDC:49967-875-025 mL in 1 PACKET
3NDC:49967-875-031.5 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(49967-875)

 
L'Oreal USA Products Inc

Medically reviewed on Nov 15, 2018

Further information

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

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