CLEARASIL ULTRA RAPID ACTION FACE SCRUB- salicylic acid lotion 
RB Health (US) LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Clearasil ® Ultra Rapid Action

Face Scrub

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.
  • 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 to three times daily if needed or as directed by a doctor
  • if bothersome dryness occurs, reduce application to once a day or every other day

Other information

  • keep tightly closed
  • store in a cool, dry place

Inactive ingredients

water, polyethylene, PPG-15 stearyl ether, glycerin, stearyl alcohol, cetyl betaine, distearyldimonium chloride, sodium lauryl sulfate, cetyl alcohol, alcohol, steareth-21, sodium chloride, behenyl alcohol, synthetic wax, steareth-2, fragrance, lavandula stoechas extract, helichrysum italicum extract, cistus monspeliensis extract, xanthan gum, dimethyl palmitamine, lauryl alcohol, mica, isopropyl alcohol, disodium EDTA, BHT, magnesium nitrate, methylchloroisothiazolinone, magnesium chloride, methylisothiazolinone, sodium sulfate, ferric ferrocyanide, titanium dioxide, FD&C blue no. 1

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 150 mL Tube Label

Clearasil®

ULTRA

Rapid Action
Face Scrub
Salicylic Acid 2% Acne Medication

12
HOURS

Visibly
clearer
skin in as
little as
12 hours

5 FL OZ (150 mL)

PRINCIPAL DISPLAY PANEL - 150 mL Tube Label
CLEARASIL ULTRA RAPID ACTION  FACE SCRUB
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-305
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)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
GLYCERIN (UNII: PDC6A3C0OX)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
CETYL BETAINE (UNII: E945X08YA9)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ALCOHOL (UNII: 3K9958V90M)  
STEARETH-21 (UNII: 53J3F32P58)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
DOCOSANOL (UNII: 9G1OE216XY)  
STEARETH-2 (UNII: V56DFE46J5)  
LAVANDULA STOECHAS FLOWERING TOP (UNII: 70759G2U6A)  
HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)  
XANTHAN GUM (UNII: TTV12P4NEE)  
DIMETHYL PALMITAMINE (UNII: 5E4QI660PW)  
LAURYL ALCOHOL (UNII: 178A96NLP2)  
MICA (UNII: V8A1AW0880)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
FERRIC FERROCYANIDE (UNII: TLE294X33A)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-305-65150 mL in 1 TUBE; Type 0: Not a Combination Product09/25/201209/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D09/25/201209/01/2020
Labeler - RB Health (US) LLC (081049410)

Revised: 5/2023
 
RB Health (US) LLC