KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT- 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

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

Inactive ingredients

water, coco-glucoside, propylene glycol, sorbitol, sodium laureth sulfate, treithanolamine, sodium chloride, PEG-120 methyl glucose dioleate, menthol, methylparaben, imidazolidinyl urea, benzophenone-4, disodium EDTA, dipropylene glycol, camphor, zinc PCA, aloe barbadensis leaf juice, boswella serrata extract, laminaria saccharina extract, blue 1, poterium officinale root extract, zinber officinale (ginger) root extract, cinnamomum cassia bark extract, hammamelis virginiana (witch hazel) leaf extract

image of a label

KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT 
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-617
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-BETAINE (UNII: 03DH2IZ3FY)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITOL (UNII: 506T60A25R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
MENTHOL (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
WITCH HAZEL (UNII: 101I4J0U34)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-617-01125 mL in 1 TUBE; Type 0: Not a Combination Product02/03/201408/12/2017
2NDC:49967-617-02200 mL in 1 TUBE; Type 0: Not a Combination Product02/03/201408/12/2017
3NDC:49967-617-03250 mL in 1 TUBE; Type 0: Not a Combination Product02/03/201408/12/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D02/03/201408/12/2017
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-617)

Revised: 1/2023
 
L'Oreal USA Products Inc