FOAMING CLEANSER- salicylic acid liquid

Foaming Cleanser by

Drug Labeling and Warnings

Foaming Cleanser 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 - 2%

PURPOSE

Purpose: Acne Treatment

DOSAGE & ADMINISTRATION

Uses:

• For the treatment of acne
• Gently cleanses and maintains optimal moisture balance
• 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 this occurs, only one medication should be used unless directed by a doctor.
  

INDICATIONS & USAGE

Directions:

• Use daily.
• Thoroughly lather foam over wet skin, rinse well and pat dry.
• Avoid eye area.
• If excessive dryness or peeling occurs, reduce application to every other day.
  

INACTIVE INGREDIENT

Water (Aqua), Alkyl (C10-16) Ether Sulfate Sodium Salt, Cocamidopropyl Betaine, Butylene Glycol, Hydrolyzed Wheat Protein, Alcohols (C12-15 Ln. saturated) Ethoxylate, Hydrolyzed Wheat Starch, Caprylyl Glycol, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sodium Hydroxide, Ethylhexyl Glycerin, Hexylene Glycol Sodium Chloride, Lavandula Angustifolia (Lavender) Leaf Oil O.E., Glycerin.

PRINCIPAL DISPLAY PANEL

Advanced Skin & Hair

Los Angeles, California 90025

877-30-CLEAR

clearogen.com

Made In USA

INGREDIENTS AND APPEARANCE

FOAMING CLEANSER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4071
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)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ROSEMARY (UNII: IJ67X351P9)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LAVENDER OIL (UNII: ZBP1YXW0H8)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4071-1	125 mL in 1 BOTTLE, PUMP

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)