FDA.reportPublic FDA data

Clearskin Professional

Manufacturer
Avon Products, Inc.
Effective date
2011-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:29:41

Label at a glance#

ProductClearskin Professional Acne Mark Treatment
Active ingredientSALICYLIC ACID
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Salicylic Acid 2.0%.....................

OTC - PURPOSE SECTION

          Purpose
............Acne Treatment

INDICATIONS & USAGE SECTION

USES

  • For the treatment of acne

WARNINGS SECTION

WARNINGS
For external use only

OTC - WHEN USING SECTION

When using this product:

  • Avoid contact with eyes. If product contacts eyes, rinse thoroughly with water. Discontinue use if excessive skin irritation develops or increases. If irritation persists, seek medical attention.
  • Using other topical acne medications at the same time or immediately after this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a health care practitioner.
  • Sunburn Alert: Use only as directed. This product contains an alpha hydroxy acid that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Please limit sun exposure and apply a sunburn protectant while using this product and for a week afterwards.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if

  • rash or irritation develops and persists

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

  • If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

  • Clean the skin thoroughly before applying this product.
  • Hold at an angle, gently rolling onto cleansed skin. Do not squeeze tube. Smooth product in with clean fingertips until fully absorbed.
  • Cover the entire affected area with a thin layer one to three times daily.
  • Because excessive drying 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

Inactive ingredients WATER/EAU, GLYCERIN, PPG-14 BUTYL ETHER, GLYCOLIC ACID, PROPANEDIOL, SODIUM HYDROXIDE, CETYL ALCOHOL, PEG-40 STEARATE, STEARETH-2, THIODIPROPIONIC ACID, SACCHAROMYCES/ZINC FERMENT, TRIOXAUNDECANEDIOIC ACID, POLYMETHYL METHACRYLATE, ORYZA SATIVA (RICE) STARCH, BIS-PEG-18 METHYL ETHER DIMETHYL SILANE, CHOLETH-24, CETETH-24, MAGNESIUM ALUMINUM SILICATE, XANTHAN GUM, DISODIUM EDTA, METHYLPARABEN, PARFUM/FRAGRANCE.

OTC - QUESTIONS SECTION

QUESTIONS? Call 1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of cartonimage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1188571clearskin Professional Acne Mark 2 % Topical CreamPSN1
317152salicylic acid 2 % Topical CreamPSN1
1188571salicylic acid 20 MG/ML Topical Cream [Clearskin Blemish]SBD1
317152salicylic acid 20 MG/ML Topical CreamSCD1
1188571Clearskin Blemish 20 MG/ML Topical CreamSY1
1188571Clearskin Emergency 2 % Topical CreamSY1
1188571Clearskin Professional Acne Mark 2 % Topical CreamSY1
317152salicylic acid 2 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0264-22019-10-29C16284748780-1960f7f55-c2a8-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0264-1Clearskin ProfessionalAcne Mark Treatment50 mL in 1 TUBECREAM501
10096-0264-2Clearskin ProfessionalAcne Mark Treatment1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0264CLEARSKIN PROFESSIONAL ACNE MARK TREATMENT (SALICYLIC ACID) CREAM [AVON PRODUCTS, INC.]1Legacy NDC, 2 package rows20110930_cb0741a3-da1f-4881-aed0-38e24b4f068d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-026410096-0264-1, 10096-0264-2

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

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
8703eef1-0559-471c-bc70-834965172d13cb0741a3-da1f-4881-aed0-38e24b4f068d2011-09-28WarningsExact identifier
spl id: 8703eef1-0559-471c-bc70-834965172d13
spl set id: cb0741a3-da1f-4881-aed0-38e24b4f068d

Reported adverse events (FAERS/openFDA)#

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