CLEARASIL ULTRA RAPID ACTION DAILY FACE WASH- salicylic acid cream

Clearasil by

Drug Labeling and Warnings

Clearasil by is a Otc medication manufactured, distributed, or labeled by Reckitt Benckiser LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only.

When using this product

• avoid contact with eyes
• 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
• if product gets into the eyes rinse thoroughly with water

Stop use and ask a doctor, if skin or eye irritation and dryness develops.

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

Directions

• wet face
• dispense product into hands and massage gently onto face
• rinse thoroughly and pat dry
• Start with one application daily, then gradually increase to two or three times daily if needed

Other information

keep tightly closed. Store in a cool, dry place.

Inactive ingredients

water, glycerin, myristic acid, stearic acid, sodium lauroyl sarcosinate, palmitic acid, potassium hydroxide, lauric acid, polyquaternium-10, fragrance, phenoxyethanol, tetrasodium EDTA, pentasodium pentetate, tetrasodium etidronate, menthol, methylparaben, butylparaben, ethylparaben, isobutylparaben, propylparaben, Aloe barbadensis leaf juice, maltodextrin, potassium sorbate, sodium benzoate

Questions?

1-866-252-5327

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Distributed by: Reckitt Benckiser LLC,
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 44 mL Tube Label

Clearasil®

ULTRA

Rapid Action
Face Wash

Salicylic Acid 2% Acne Medication

MAXIMUM STRENGTH

1.5 FL. OZ. (44 mL)

INGREDIENTS AND APPEARANCE

CLEARASIL   ULTRA RAPID ACTION DAILY FACE WASH
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-326
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
MYRISTIC ACID (UNII: 0I3V7S25AW)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
PALMITIC ACID (UNII: 2V16EO95H1)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
LAURIC ACID (UNII: 1160N9NU9U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE SODIUM (UNII: MP1J8420LU)
PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
ETHYLPARABEN (UNII: 14255EXE39)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-326-44	44 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	03/01/2016

Labeler - Reckitt Benckiser LLC (094405024)