CLARIFYING FACE AND BODY WASH- benzoyl peroxide liquid

Clarifying Face and Body Wash by

Drug Labeling and Warnings

Clarifying Face and Body Wash by is a Otc medication manufactured, distributed, or labeled by Acneology Treatment Center, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzoyl Peroxide 2.5%

Purpose

For the treatment of acne

Uses

Adults and children 12 years and over:

• For the treatment of acne
• For acne-prone or oily skin

Warnings

For external use only. Avoid contact with eyes and eyelids. This product may cause irritation. Mild irritation may be reduced by using the product less frequently. If irritation becomes severe, discontinue use and consult a doctor.

Do not use

this product if you have very sensitive skin or if you are sensitive to benzoyl peroxide.

Keep out of reach of children

• If swallowed, get medical help or contacting Poison Control Center right away.

Directions

Use 1 to 3 times daily on affected skin, work into lather, rinse off thoroughly.

Other Information

• May bleach hair or fabrics.
• Store at room temperature.
• Keep away from heat or direct sunlight.

Inactive Ingredients

Purified Water, Ammonium Lauryl Sulfate, Glycerin, Disodium Cocoamphodiacetate, Propylene Glycol, Carbomer, Sodium Hydroxide.

Questions or Comments?

Call Toll-Free 800-439-4166

Package Labeling:

INGREDIENTS AND APPEARANCE

CLARIFYING FACE AND BODY WASH 
benzoyl peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73610-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	25 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
GLYCERIN (UNII: PDC6A3C0OX)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73610-000-00	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	03/16/2020

Labeler - Acneology Treatment Center, LLC (047568655)