KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION- salicylic acid liquid

Kiehls Since 1851 Dermatologist Solutions Truly Targeted Acne Clearing Solution by

Drug Labeling and Warnings

Kiehls Since 1851 Dermatologist Solutions Truly Targeted Acne Clearing Solution by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, L'Oreal USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

• for the treatment of acne
• helps clear up acne blemishes and allows skin to heal

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, gluconolactone, niacinamide, butylene glycol, glycolic acid, sodium hydroxide, glycerin, methyl gluceth-20, hydroxyethylcellulose, caprylyl glycol, dipotassium glycyrrhizate

Questions or comments?

Call toll-free 1-800-946-4453

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-055
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
NIACINAMIDE (UNII: 25X51I8RD4)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCOLIC ACID (UNII: 0WT12SX38S)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCERIN (UNII: PDC6A3C0OX)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-055-01	1 in 1 CARTON	06/01/2023
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 49967-055-02	4 mL in 1 VIAL; Type 0: Not a Combination Product	06/01/2023
3	NDC: 49967-055-03	2 mL in 1 PACKET; Type 0: Not a Combination Product	06/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	06/01/2023

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA, Inc.		185931458	manufacture(49967-055) , pack(49967-055)