Clear Exfoliating Solution

Manufacturer
Cosmetic Enterprises Ltd
Effective date
2025-10-10
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:38:52

Label at a glance#

ProductClear Exfoliating Solution Paulas Choice
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredeints                   Purpose

Salicylic Acd 2.0% ................... Acne Treatment

OTC - PURPOSE SECTION

Uses

  • For the treatment of acne
  • Penetrates Pores to eliminate most acne blemishes, blackheads, and whiteheads
  • Helps prevent new acne blemishes, blackheads and whiteheads

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Stop use and ask a doctorif skin irritation occurs or gets worse

WARNINGS SECTION

Warning

  • For external use only
  • When using this product 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
    

DOSAGE & ADMINISTRATION SECTION

DirectionsAfter cleansing with Paula's Choice Clear Pore Normalizing Cleanser

  • Cover the entire affected area with a thin layer one to three times daily
  • Because excessive drying out 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 

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAULA'S CHOICE

CLEAR

ANTI-REDNESS

EXFOLIATING SOLUTION

2% Salicylic Acid

All Skin Types

What it does:

  • Clears breakouts
  • Unclogs & Minimizes pores
  • Fades red marks

118 ml / 4 fl. oz.

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
317152salicylic acid 2 % Topical CreamPSN5
317152salicylic acid 20 MG/ML Topical CreamSCD5
317152salicylic acid 2 % Topical CreamSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130655439062008GTIN-13: 0655439062008
EAN-13: 0655439062008
GTIN-12: 655439062008
UPC-A: 655439062008
GTIN storage (14 digits): 00655439062008
6200_Component.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56152-5002-1Clear Exfoliating SolutionPaulas Choice118 mL in 1 TUBECREAM1185
56152-5002-2Clear Exfoliating SolutionPaulas Choice15 mL in 1 TUBECREAM155

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56152-500256152-5002-1, 56152-5002-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-11-04full-release2026-06-01 00:34:01

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Clear Exfoliating Solution Paulas ChoiceSALICYLIC ACIDCosmetic Enterprises Ltdf84a2b7e-1e02-450f-b290-b4f6f87cdb7a2025-10-10WarningsExact identifier
ndc (package): 56152-5002-1
ndc (package): 56152-5002-2
ndc (product): 56152-5002
ndc11 (package): 56152500202
ndc11 (package): 56152500201
spl id: 40d3c232-3cb0-81e9-e063-6394a90aa452
spl set id: f84a2b7e-1e02-450f-b290-b4f6f87cdb7a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.