KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT- salicylic acid lotion 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient


Salicylic acid 1.5%

Purpose

Acne treatment

Use

for the treatment of acne

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

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, sodium hydroxide, citric acid, hydrogenated coconut acid, capryloyl salicylic acid, coconut acid, sodium PCA, camphor, menthol, boswellia serrata resin 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

Questions or comments?

Call toll free 1-800-946-4453

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KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-618
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID15 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCO GLUCOSIDE (UNII: ICS790225B)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCO-BETAINE (UNII: 03DH2IZ3FY)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
COCONUT ACID (UNII: 40U37V505D)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
MENTHOL (UNII: L7T10EIP3A)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
SODIUM ISETHIONATE (UNII: 3R36J71C17)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALCOHOL (UNII: 3K9958V90M)  
GINGER (UNII: C5529G5JPQ)  
SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
CHINESE CINNAMON (UNII: WS4CQ062KM)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-618-0175 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2017
2NDC:49967-618-02150 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2017
3NDC:49967-618-0330 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2017
4NDC:49967-618-043 mL in 1 PACKET; Type 0: Not a Combination Product03/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00603/01/2017
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-618) , pack(49967-618)

Revised: 12/2023
Document Id: ed72f45f-ed6f-446a-b244-38308c03662f
Set id: 09e7f362-6187-4e49-b703-8249c70e5124
Version: 5
Effective Time: 20231230
 
L'Oreal USA Products Inc