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Kiehls Since 1851 Blue Herbal Acne Cleanser Treatment

Dosage form: lotion
Ingredients: SALICYLIC ACID 15mg in 1mL
Labeler: L'Oreal USA Products Inc
NDC Code: 49967-618

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%


Acne treatment


for the treatment of acne


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.

  • wet face, then work product into a lather
  • massage onto face avoiding the eye area
  • rinse well
  • use twice daily

Inactive ingredients

water, coco-glucoside, propylene glycol, ammonium polyacryloyldimethyl taurate, glycerin, coco-betaine, sodium cocoyl isethionate, sodium methyl cocoyl taurate, dipropylene glycol, sodium chloride, butylene glycol, phenoxyethanol, hydrogenated coconut acid, capryloyl salicylic acid, coconut acid, t-butyl alcohol, sodium PCA, camphor, menthol, boswellia serrata extract, sodium isethionate, hamamelis virginiana (witch hazel) water, peumus boldus leaf extract, disodium EDTA, alcohol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, xanthan gum, laminaria saccharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

Questions or comments?

Call toll free 1-800-946-4453

salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-618
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:49967-618-0175 mL in 1 TUBE
2NDC:49967-618-02150 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/01/2017
Labeler - L'Oreal USA Products Inc (002136794)
L'Oreal USA, Inc.185931458manufacture(49967-618)

Revised: 11/2016
L'Oreal USA Products Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.