DETOX DROPS 2% SALICYLIC ACID ACNE TONER- salicylic acid liquid

Detox Drops 2% Salicylic Acid Acne Toner by

Drug Labeling and Warnings

Detox Drops 2% Salicylic Acid Acne Toner by is a Otc medication manufactured, distributed, or labeled by COSMAX USA, CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid 2%

PURPOSE

Purpose

Acne medication

USES

Use

For the treatment of acne. Clears acne blemishes and allows skin to heal. Helps prevent the development of new blemishes.

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
• avoid contact with eyes
• if eye contact occurs, flush thoroughly with water

WARNINGS

Warnings

For external use only.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Directions

• shake well before use
• clean 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 increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

OTHER INFORMATION

Other information

Store at room temperature

INACTIVE INGREDIENT

Inactive Ingredients

WATER, JUNIPERUS COMMUNIS FRUIT EXTRACT, POLYSORBATE 20, METHYLPROPANEDIOL, LACTOBACILLUS/SALIX PURPUREA BARK FERMENT EXTRACT, BUTYLENE GLYCOL, GLYCERIN, SODIUM HYDROXIDE, DECYL GLUCOSIDE, MENTHYL LACTATE, LACTOBACILLUS FERMENT, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, LAURYL GLUCOSIDE, CITRIC ACUD, LACTIC ACID.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DETOX DROPS 2% SALICYLIC ACID ACNE TONER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68577-189
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CITRIC ACID (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
GLYCERIN (UNII: PDC6A3C0OX)
CUCUMIS SATIVUS (CUCUMBER) FRUIT (UNII: YY7C30VXJT)
LACTIC ACID (UNII: 33X04XA5AT)
LIMOSILACTOBACILLUS FERMENTUM ME-3 (UNII: BQX4W45LG8)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
JUNIPER BERRY (UNII: O84B5194RL)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
MENTHYL LACTATE (UNII: 2BF9E65L7I)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68577-189-00	1 in 1 CARTON	10/01/2024
1		120 mg in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	10/01/2024

Labeler - COSMAX USA, CORPORATION (010990210)

Establishment
Name	Address	ID/FEI	Business Operations
COSMAX USA, CORPORATION		010990210	manufacture(68577-189)