CLARIFYING TONER- salicylic acid liquid

Clarifying Toner by

Drug Labeling and Warnings

Clarifying Toner by is a Otc medication manufactured, distributed, or labeled by Allure Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:

Salicylic Acid - 1%

PURPOSE

Purpose: Acne Treatment

INDICATIONS & USAGE

Uses:

• For the treatment of acne.
• Eliminates pore clogging impurities.
• For all skin types.
  

WARNINGS

Warnings:

For external use only

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

WHEN USING

• Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.
• If excessive irritation occurs reduce application to once a day.
  

DOSAGE & ADMINISTRATION

Directions:

• Cleanse the skin thoroughly before applying medication.
• Avoid eye area.
• If excessive irritation, drying or peeling occurs, reduce application to once a day.
  

INACTIVE INGREDIENT

Water (Aqua), SD Alcohol 40-B (Alcohol Denat.), Hamamelis Virginiana (Witch Hazel)  Water, Glycerine, Polysorbate 20, Symphytum Officinale (Comfrey)  Extract, Plantago Ovata (Indian Plantin) Seed Extract, Sodium PCA, Hydrolyzed Wheat Protein, Hydrolyzed Wheat Starch, Phenoxyethanol, Caprylyl Glycol, Ethylhexyl Glycerin, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Chamomile) Flower Extract, Hexylene Glycol, Allantoin, Dipotassium Glycyrrhizate.

PRINCIPAL DISPLAY PANEL

Advanced Skin Care

Los Angeles, California 90025

877-20-CLEAR

clearogen.com

made in USA

INGREDIENTS AND APPEARANCE

CLARIFYING TONER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
COMFREY ROOT (UNII: M9VVZ08EKQ)
PLANTAGO OVATA SEED (UNII: UD50RBY30F)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ROSEMARY (UNII: IJ67X351P9)
CHAMOMILE (UNII: FGL3685T2X)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ALLANTOIN (UNII: 344S277G0Z)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4070-1	120 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	06/07/2014

Labeler - Allure Labs, Inc (926831603)