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

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.

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

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KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT
salicylic acid lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-617
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
COCO-BETAINE
PROPYLENE GLYCOL
SORBITOL
SODIUM LAURETH SULFATE
SODIUM CHLORIDE
PEG-120 METHYL GLUCOSE DIOLEATE
MENTHOL
METHYLPARABEN
DIPROPYLENE GLYCOL
CAMPHOR (SYNTHETIC)
WITCH HAZEL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49967-617-01 125 mL in 1 TUBE None
2 NDC:49967-617-02 200 mL in 1 TUBE None
3 NDC:49967-617-03 250 mL in 1 TUBE 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 (49967-617)

Revised: 01/2020 L’Oreal USA Products Inc

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