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

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Clearasil ®Ultra
Acne + Marks Daily Scrub

Drug Facts

Active ingredient

2% Salicylic acid

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 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

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, sodium cocoyl isethionate, glycerin, cetyl alcohol, laureth-3, polyethylene, sodium laureth sulfate, sodium cocoamphoacetate, niacinamide, sodium lactate, sorbitol, hexyldecanol, fragrance, acrylates C10-30 alkyl acrylate crosspolymer, sodium hydroxide, dipotassium glycrrhizate, disodium EDTA, bisabolol, cetylhydroxyproline palmitamide, stearic acid, polyquaternium-43, brassica campestris (rapeseed) sterols, phenoxyethanol, methylparaben, butylparaben, ethylparaben, isobutylparaben, propylparaben, FD&C blue no. 1, FD&C yellow no. 6

Questions?

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 - 150 mL Tube Label

NEW

Clearasil®

ULTRA

Acne + Marks
Daily Scrub

Salicylic Acid 2% Acne Medication

REDUCES
MARKS

Helps clear
pimples fast,
and reduces the
appearance of
acne marks

5.0 FL OZ (150 mL)

Principal Display Panel - 150 mL Tube Label
CLEARASIL ULTRA  ACNE PLUS MARKS DAILY SCRUB
salicylic acid lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-395
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
LAURETH-3 (UNII: F32E4CB0UJ)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
NIACINAMIDE (UNII: 25X51I8RD4)  
SODIUM LACTATE (UNII: TU7HW0W0QT)  
SORBITOL (UNII: 506T60A25R)  
HEXYLDECANOL (UNII: 151Z7P1317)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LEVOMENOL (UNII: 24WE03BX2T)  
CETYLHYDROXYPROLINE PALMITAMIDE (UNII: 74ONU0S62G)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
RAPESEED STEROL (UNII: B46B6DD20U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
ETHYLPARABEN (UNII: 14255EXE39)  
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63824-395-65150 mL in 1 TUBE; Type 0: Not a Combination Product05/04/201209/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00605/04/201209/01/2024
Labeler - RB Health (US) LLC (081049410)

Revised: 10/2023
Document Id: 06fd70ae-8e12-90b7-e063-6294a90a0622
Set id: b6779e34-cadc-4fa5-bc0e-5e9a2ccd3f52
Version: 3
Effective Time: 20231005
 
RB Health (US) LLC