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

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Drug Facts

Active ingredient


Salicylic acid 2%

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, alcohol denat., glycerin, butylene glycol, methyl methacrylate crosspolymer, ammonium polyacryloyldimethyl taurate, perlite, nylon-12, dipropylene glycol, xanthan gum, peumus boldus leaf extract, boswellia serrata extract, hamamelis virginiana (witch hazel) water, t-butyl alcohol, camphor, menthol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, phenoxyethanol, cinnamal, laminaria accharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

Questions or comments?

Call toll-free 1-800-946-4453

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KIEHLS SINCE 1851 BLUE HERBAL ACNE SPOT TREATMENT 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-527
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)  
PERLITE (UNII: 0SG101ZGK9)  
NYLON-12 (UNII: 446U8J075B)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
MENTHOL (UNII: L7T10EIP3A)  
GINGER (UNII: C5529G5JPQ)  
SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
CHINESE CINNAMON (UNII: WS4CQ062KM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CINNAMALDEHYDE (UNII: SR60A3XG0F)  
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
ZINC SULFATE (UNII: 89DS0H96TB)  
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-527-011 in 1 CARTON08/31/201602/07/2025
115 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49967-527-021.5 mL in 1 PACKET; Type 0: Not a Combination Product08/31/201602/07/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/31/201602/07/2025
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458analysis(49967-527)
Establishment
NameAddressID/FEIBusiness Operations
Cosmetic Essence, LLC dba Voyant Beauty032565959manufacture(49967-527)
Establishment
NameAddressID/FEIBusiness Operations
Paklab078717086pack(49967-527)

Revised: 12/2023
Document Id: f7bd47b0-d8ad-4abe-92ea-734a7ffcc2f8
Set id: e74e09d1-ebef-4c44-9a11-c703a87a3c25
Version: 4
Effective Time: 20231230
 
L'Oreal USA Products Inc