SO CLEAR REPAIR SPOT TREATMENT liquid

So Clear Repair Spot Treatment by

Drug Labeling and Warnings

So Clear Repair Spot Treatment by is a Otc medication manufactured, distributed, or labeled by RemeVerse LLC, Lexia LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

So Clear Repair Spot Treatment

Benzoyl Peroxide 5.0%

So Clear Repair Spot Treatment

Water, Magnesium Aluminum Silicate, Allantoin, Polysorbate-20, Sodium Hydroxide, Carbomer, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol

Directions

After using So Clear Cleanse and Protect, apply to acne blemishes. Allow to dry. Do not wash off. 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 become severe

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

STOP USE

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

PURPOSE

Acne treatment

Other Information

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

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center right away

So Clear Repair

INGREDIENTS AND APPEARANCE

SO CLEAR REPAIR SPOT TREATMENT 
so clear repair spot treatment liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70317-148
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	0.7875 g  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CARBOMER 940 (UNII: 4Q93RCW27E)
ALLANTOIN (UNII: 344S277G0Z)
OCTYLPHENOXYETHANOL (UNII: 5G75D69KFO)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Characteristics
Color		Score
Shape	ROUND	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70317-148-15	15 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 LLC (050186540)

Registrant - Lexia LLC (015552120)

Establishment
Name	Address	ID/FEI	Business Operations
Lexia LLC		015552120	manufacture(70317-148)