PAULAS CHOICE CLEAR ANTI REDNESS EXFOLIATING SOLUTION- salicylic acid liquid 
Paula's Choice, 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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Paulas Choice CLEAR Anti-Redness Exfoliating Solution 2% Salicylic Acid, Regular Strength

Salicylic Acid

After cleansing with Paula's Choice Clear Pore Normalizing Cleanser, soak a large cotton ball with Regular Strength Anti-Redness Exfoliating Solution and gently stroke over the face, paying special attention to acne and blackhead prone areas. Do not rinse. Avoid contact with eyes, eyelids, and mucous membranes. If contact occurs, rinse with water. If excessive dryness or peeling occurs, reduce application to once per day or once every other day.

If contact occurs, rinse with water. If excessive dryness or peeling occurs, reduce application to once per day or once every other day.

Warnings

For external use only.

Do not use

Stop use and ask a doctor if too much skin irritation or skin sensitivity develops or increases.

When using this product

· Do not use in or near the eyes

· Using other topical acne products at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.

Keep out of reach of children. If swallowed, get medical help and contact a Poison Control Center immediately.

Water, Dipropylene Glycol, Pentylene Glycol, Polysorbate 20, Butylene Glycol, Glycerin, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Allantoin. Panthenol, PEG/PPG-17/6 Copolymer, Methyl Gluceth-20, Glycereth-26, Bis-PEG-18 Methyl Ether Dimethyl Silane, Sodium Hydroxide, Sodium Metabisulfite, Tetrasodium EDTA

Full Size Component Label

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PAULAS CHOICE CLEAR ANTI REDNESS EXFOLIATING SOLUTION 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76144-620
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)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
GLYCERETH-26 (UNII: NNE56F2N14)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE SODIUM (UNII: MP1J8420LU)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
ALLANTOIN (UNII: 344S277G0Z)  
PANTHENOL (UNII: WV9CM0O67Z)  
PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259)  
BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76144-620-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/17/2009
2NDC:76144-620-0230 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package01/14/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/17/2009
Labeler - Paula's Choice, LLC. (029583981)

Revised: 6/2022
Document Id: c54e1794-a620-5163-e053-2995a90a4725
Set id: 19ac69ad-d2b7-3aaa-e054-00144ff88e88
Version: 4
Effective Time: 20220606
 
Paula's Choice, LLC.