Kiehls Since 1851 Blue Herbal Spot Treatment Acne: Package Insert and Label Information

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.

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

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KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE
salicylic acid lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-615
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID 15 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
ALCOHOL
GLYCERIN
GLYCOLIC ACID
TROLAMINE
PENTYLENE GLYCOL
DIPROPYLENE GLYCOL
CAMPHOR (NATURAL)
MENTHOL
WITCH HAZEL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49967-615-01 1 TUBE in 1 CARTON contains a TUBE
1 15 mL in 1 TUBE This package is contained within the CARTON (49967-615-01)
2 NDC:49967-615-02 1.5 mL in 1 PACKET None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 02/03/2014
Labeler — L’Oreal USA Products Inc (002136794)
Establishment
Name Address ID/FEI Operations
L’Oreal USA, Inc. 185931458 manufacture (49967-615)

Revised: 01/2020 L’Oreal USA Products Inc

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