SO CLEAR CLEANSE ACNE CLEANSER- benzoyl peroxide liquid

So Clear Cleanse Acne Cleanser by

Drug Labeling and Warnings

So Clear Cleanse Acne Cleanser by is a Otc medication manufactured, distributed, or labeled by RemeVerse, Lexia LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

So Clear Cleanse Acne Cleanser

Benzoyl Peroxide

So Clear Cleanse Acne Cleanser

Water, Disodium Laureth Sulfosuccinate, Sodium Cocoyl Isethionate, Cocamidopropyl Betaine, Acrylates Copolymer, Magnesium Aluminum Silicate, Sodium Xylenesulfonate, Montan Wax, Glycolic Acid, Sodium C14-16 Alpha Olefin Sulfonate, Sodium Hydroxide, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol

Directions

Starting with clean hands, apply to face, nose, or ears and gently rub in. Apply 1 -2 times daily. Discontinue use if increased irritation occurs.

Uses

for management of acne

SPL UNCLASSIFIED SECTION

Store at room temperature. Avoid high excessive heat. (99 degrees F)

WARNINGS

Warnings

For external use only

Do not use this medication if you are sensitive to Benzoyl Peroxide.

When using this product § Avoid unnecessary sun exposure and use a sunscreen. § Avoid contact with eyes, lips and mouth. § 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.

Skin irritation may occur, characterized by redness, burning, itching, peeling or possible swelling. Irritation may be reduced by using this product less frequently or in a lower concentration.

Stop use and ask a doctor if skin irritation becomes severe.

Stop Use Section

Stop use and ask a doctor if skin irritation becomes severe.

So Clear Cleanse Acne Cleanser

Acne treatment

Keep out of the reach of Children

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

So Clear Cleanser

INGREDIENTS AND APPEARANCE

SO CLEAR CLEANSE ACNE CLEANSER 
benzoyl peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70317-146
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	3.6 g  in 120 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCOLIC ACID (UNII: 0WT12SX38S)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
MONTAN WAX (UNII: N2TH4S4KUD)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70317-146-04	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	03/31/2021

Labeler - RemeVerse (050186540)

Registrant - Lexia LLC (015552120)

Establishment
Name	Address	ID/FEI	Business Operations
Lexia LLC		015552120	manufacture(70317-146)