KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL ACNE TREATMENT FACIAL- salicylic acid lotion 
L'Oreal USA Products Inc

----------

Drug Facts

Active ingredient

Salicylic acid 1.5%

Purpose

Acne treatment

Uses

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, 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?

Call toll free 1-800-946-4453

image of a carton

image of a carton
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 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)  
NIACINAMIDE (UNII: 25X51I8RD4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG)  
CITRAL (UNII: T7EU0O9VPP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-875-011 in 1 CARTON11/01/201611/01/2016
160 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49967-875-025 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
3NDC:49967-875-031.5 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
4NDC:49967-875-045 mL in 1 TUBE; Type 0: Not a Combination Product11/01/2016
5NDC:49967-875-051 in 1 CARTON11/01/2016
560 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00611/01/2016
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-875) , pack(49967-875)

Revised: 12/2023
Document Id: ee0f43e2-ca94-44d7-a4ff-cc1e71929f4b
Set id: 3346f5f8-5793-47f6-8e71-250d3cc05c0d
Version: 7
Effective Time: 20231230
 
L'Oreal USA Products Inc