CLEARASIL ULTRA RAPID ACTION DAILY WASH- salicylic acid gel

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]

SPL UNCLASSIFIED SECTION

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 the eyes. If product gets into the eyes rinse thoroughly with water.
• Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation. If this occurs, only one medication should be used unless directed by a doctor.

Stop use and ask a doctor if skin or eye irritation 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

store in a cool, dry place

Inactive ingredients

water, glycerin, sodium laureth sulfate, coco-glucoside, cocamidopropyl betaine, PEG-200 hydrogenated glyceryl palmate, sodium chloride, laureth-4, PEG-7 glyceryl cocoate, polyquaterium-43, fragrance, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract, sodium hydroxide, phenoxyethanol, sodium benzoate, FD&C blue no. 1

Questions?

1-866-25-CLEAR (1-866-252-5327)

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 200 mL Bottle Label

Clearasil®

ULTRA

Rapid Action
Gel Wash
Salicylic Acid 2% Acne Medication

MAXIMUM STRENGTH

12
HRS
Visibly
clearer skin
in as fast as
12 hours

6.78 FL. OZ. (200 mL)

INGREDIENTS AND APPEARANCE

CLEARASIL   ULTRA RAPID ACTION DAILY WASH
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63824-355
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)
sodium laureth-3 sulfate (UNII: BPV390UAP0)
coco glucoside (UNII: ICS790225B)
cocamidopropyl betaine (UNII: 5OCF3O11KX)
PEG-200 hydrogenated glyceryl palmate (UNII: W161T051Y1)
sodium chloride (UNII: 451W47IQ8X)
laureth-4 (UNII: 6HQ855798J)
PEG-7 glyceryl cocoate (UNII: VNX7251543)
helichrysum italicum flower (UNII: P62Y550X24)
sodium hydroxide (UNII: 55X04QC32I)
phenoxyethanol (UNII: HIE492ZZ3T)
sodium benzoate (UNII: OJ245FE5EU)
FD&C blue no. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63824-355-01	200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	06/01/2016

Labeler - Reckitt Benckiser LLC (094405024)