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

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.

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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

  • 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 ingrease to two or three times dialy if neded or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl

Inactive ingredients

water, alcohol denat., glycerin, glycolic acid, triethanolamine, ammonium polyacryloyldimethyl taurate, acrylates/C10-30 alkyl acrylate crosspolymer, pentylene glycol, butylene glycol, zinc gluconate, propylelne glycol, dipropylene glycol, camphor, menthol, aloe barbadensis leaf juice, boswellia serrata extract, laminaria saccharina extract, hammamelis viginiana (witch hazel) leaf extract, potarium officinale root exract, zingiber officinale (ginger) root extract, cimmamoum casaia bark extract

image of a label

KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-615
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)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
TROLAMINE (UNII: 9O3K93S3TK)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
MENTHOL (UNII: L7T10EIP3A)  
WITCH HAZEL (UNII: 101I4J0U34)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-615-011 in 1 CARTON02/03/201412/29/2017
115 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49967-615-021.5 mL in 1 PACKET; Type 0: Not a Combination Product02/03/201412/29/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D02/03/201412/29/2017
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-615)

Revised: 12/2021
 
L'Oreal USA Products Inc