CLEARASIL ULTRA RAPID ACTION CLEAR SKIN- salicylic acid and benzoyl peroxide 
RB Health (US) LLC

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Clearasil ®
Ultra™ Rapid Action Clear Skin

Drug Facts

Rapid Action Daily Face Wash

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.
  • 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.
  • limit use to the face and neck

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 and neck, avoiding the delicate eye area
  • cover the entire affected area with a thin layer and rinse thoroughly with warm water one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other information

  • store in a cool, dry place
  • do not freeze

Inactive ingredients

water, sodium cocoyl isethionate, cetearyl alcohol, glycerin, sodium laureth sulfate, sodium cocoamphoacetate, cocamidopropyl betaine, sodium hydroxide, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, disodium EDTA, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract

Rapid Action Pads

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

Flammablekeep away from extreme heat or open flame

When using this product

  • avoid contact with the eyes. If product gets into the eyes rinse thoroughly with water.
  • 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.
  • limit use to the face and neck

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

Directions

  • clean the skin thoroughly before applying this product
  • wipe a pad over face and neck to cover the entire affected area with a thin layer 1 to 3 times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other information

  • keep jar lid tightly closed
  • store in a cool, dry place but do not freeze

Inactive ingredients

water, alcohol denat., glycerin, isoceteth-20, sorbitol, sodium hydroxide, fragrance, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract, disodium EDTA

Rapid Action Vanishing Treatment Cream

Active ingredient

Benzoyl Peroxide 10%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

Do not useif you have very sensitive skin or are sensitive to benzoyl peroxide

When using this product

  • avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with the eyes, lips and mouth
  • avoid contact with hair or dyed fabrics, including carpet and clothing which may be bleached by this product
  • with other topical acne medications, at the same time or immediately following use of this product, increased dryness or irritation of the skin may occur. If this occurs, only one medication should be used unless directed by a doctor.
  • skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. More frequent use or higher concentrations may aggravate skin irritation. Mild irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor ifskin irritation becomes severe

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • cleanse the skin thoroughly before applying medication
  • cover the entire affected area with a thin layer one to three times daily
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • if going outside, use a sunscreen.Allow ClearasilUltra® Rapid Action Vanishing Treatment Cream to dry, then follow directions on sunscreen labeling. If irritation or sensitivity develops, discontinue use of both products and ask a doctor

Other information

  • keep tightly closed
  • store at controlled room temperature 68-77°F (20-25°C)

Inactive ingredients

water, gluconolactone, glyceryl stearate, glycerin, PEG-40 stearate, PEG-100 stearate, cetyl alcohol, dimethicone, magnesium aluminum silicate, xanthan gum, phenoxyethanol, ammonium hydroxide, isopropylparaben, butylparaben, isobutylparaben, arginine, titanium dioxide

Questions?

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

You may also report side effects to this phone number.

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

PRINCIPAL DISPLAY PANEL - Kit Carton

Clearasil®

ULTRA™

Rapid Action
Clear Skin Kit

MAXIMUM
STRENGTH

Visibly
clearer skin
in as little as
12 hours

  • Clearasil Ultra Rapid
    Action Daily Face Wash
    6.78 FL. OZ. (200 mL)
  • Clearasil Ultra Rapid
    Action Pads
    90 Pads 3.58 in 2(23.1 cm 2)
  • Clearasil Ultra Rapid
    Action Treatment Cream
    0.45 OZ. (13 g)
PRINCIPAL DISPLAY PANEL - Kit Carton
CLEARASIL  ULTRA RAPID ACTION CLEAR SKIN
salicylic acid and benzoyl peroxide kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-423
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-423-001 in 1 CARTON; Type 0: Not a Combination Product07/01/201509/01/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 200 mL
Part 21 JAR 90 
Part 1 of 2
CLEARASIL ULTRA RAPID ACTION  DAILY FACE WASH
salicylic acid lotion
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)  
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-380-88200 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00609/01/2014
Part 2 of 2
CLEARASIL ULTRA  RAPID ACTION PADS
salicylic acid solution
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.03 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOCETETH-20 (UNII: O020065R7Z)  
SORBITOL (UNII: 506T60A25R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)  
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
Product Characteristics
Color    Score    
ShapeROUND (Pad) Size231mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-345-0190 in 1 JAR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00606/01/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00607/01/201509/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
 
RB Health (US) LLC