CLEARASIL ULTRA ACNE PLUS MARKS SPOT- salicylic acid lotion 
RB Health (US) LLC

----------

Clearasil ®Ultra
Acne+Marks Spot Lotion

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, lips and mouth. If contact occurs, 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
  • Wash hands after use
  • Sun Alert:Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use

Stop use and ask a doctor ifskin or eye irritation develops.

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

Directions

Other information

Inactive ingredients

Water, Alcohol Denat., Octyldodecanol, Dimethicone, Niacinamide, Sodium Lactate, Isohexadecane, Polyacrylamide, Sodium Hydroxide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Hexyldecanol, C13-14 Isoparaffin, Magnesium Aluminum Silicate, Fragrance, Laureth-7, Disodium EDTA, Dipotassium Glycyrrhizate, Bisabolol, Cetylhydroxyproline Palmitamide, Stearic Acid, Brassica Campestris (Rapeseed) Sterols, 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
Made in USA

PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton

Clearasil ®

ULTRA

Acne + Marks
Spot Lotion
Salicylic Acid 2% Acne Medication

REDUCES
MARKS

Helps to clear
pimples fast
and reduce the
appearance of
acne marks

1 FL. OZ. (30 mL)

PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton
CLEARASIL ULTRA  ACNE PLUS MARKS SPOT
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-347
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)  
OCTYLDODECANOL (UNII: 461N1O614Y)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
NIACINAMIDE (UNII: 25X51I8RD4)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
HEXYLDECANOL (UNII: 151Z7P1317)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
LAURETH-7 (UNII: Z95S6G8201)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LEVOMENOL (UNII: 24WE03BX2T)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-347-011 in 1 CARTON08/01/201109/01/2024
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/01/201109/01/2024
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
Document Id: 06fd3608-5f62-dbcc-e063-6394a90a38a6
Set id: e85e14fb-afb1-49b9-b33e-c35aabbf5652
Version: 4
Effective Time: 20231005
 
RB Health (US) LLC