FDA.reportPublic FDA data

Clearskin Blackhead Eliminating

Manufacturer
New Avon LLC | Avon Products, Inc.
Effective date
2016-02-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:45:20

Label at a glance#

ProductClearskin Blackhead Eliminating Daily Astringent
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
  • helps clear up blackheads
  • helps prevent new blackheads from forming

WARNINGS SECTION

​Warnings

​For external use only.

OTC - WHEN USING SECTION

​When using this product

  • ​avoid contact with eyes. 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, use only one topical acne medication at a time unless directed by a health care practitioner.
OTC - STOP USE SECTION

​Stop use and ask a health care practitioner if​ rash or irritation develops or increases.

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.
GENERAL PRECAUTIONS SECTION

Flammable. Keep away from heat or flame. Keep out of direct sunlight.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Cleanse the skin thoroughly before applying the product.
  • Moisten cotton ball and cover the entire affected area with a thin layer one to three times daily.
  • Gently work moistened cotton ball over face and neck. Do not rinse.
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a health care practitioner.
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

GENERAL PRECAUTIONS SECTION

DO NOT USE IF SEAL IS BROKEN.

INACTIVE INGREDIENT SECTION

Inactive ingredients SD alcohol 40-B, water/eau, propylene glycol, PEG-6, potassium hydroxide, benzophenone-1, parfum/fragrance, BHT, disodium EDTA, lysine carboxymethyl cysteinate, isododecane, aloe barbadensis leaf juice, sodium C8-16 isoalkylsuccinyl lactoglobulin sulfonate, polystyrene/
hydrogenated polyisopentene copolymer, chamomilla recutita (matricaria) flower extract, blue 1/CI 42090, red 33/CI 17200.

OTC - QUESTIONS SECTION

Questions? Call 1-800-FOR-AVON or 1-800-265-AVON in Canada.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of back labelimage of back labelimage of back labelimage of back label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053276clearskin for Blackheads Astringent 2 % Topical SolutionPSN2
251577salicylic acid 2 % Topical SolutionPSN2
1053276salicylic acid 20 MG/ML Topical Solution [Clearskin Blemish]SBD2
251577salicylic acid 20 MG/ML Topical SolutionSCD2
1053276Clearskin Blackhead Eliminating 2 % Daily AstringentSY2
1053276Clearskin Blemish 20 MG/ML Topical SolutionSY2
251577salicylic acid 2 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0320-12020-01-31C16284748780-19d75b9cf-db1d-f424-e053-dadaa90a57ce5ad5f4b3-70c2-419a-bb41-ca092b20ac62

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0320-1Clearskin Blackhead EliminatingDaily Astringent250 mL in 1 BOTTLELIQUID2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0320CLEARSKIN BLACKHEAD ELIMINATING DAILY ASTRINGENT (SALICYLIC ACID) LIQUID [NEW AVON LLC]2Legacy NDC, 1 package rows20160307_5ad5f4b3-70c2-419a-bb41-ca092b20ac62.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
10096-032010096-0320-1

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
1208738f-722f-420f-a324-8a819546715b5ad5f4b3-70c2-419a-bb41-ca092b20ac622016-02-19WarningsExact identifier
spl id: 1208738f-722f-420f-a324-8a819546715b
spl set id: 5ad5f4b3-70c2-419a-bb41-ca092b20ac62

Reported adverse events (FAERS/openFDA)#

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