FDA.reportPublic FDA data

ACNE SOLUTIONS CLEARING CONCEALER

Manufacturer
CLINIQUE LABORATORIES INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:09

Label at a glance#

ProductACNE SOLUTIONS CLEARING CONCEALER ACNE MEDICATION ALL SKIN TYPES
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


ACTIVE INGREDIENT: 1.0% SALICYLIC ACID

OTC - PURPOSE SECTION

PURPOSE: ACNE TREATMENT

USE: TREATS ACNE

WARNINGS SECTION

WARNINGS: FOR EXTERNAL USE ONLY. AVOID EYE AREA

OTC - WHEN USING SECTION


WHEN USING THIS PRODUCT: USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

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
  • CLEANSE SKIN THOROUGHLY BEFORE APPLYING
  • COVER THE ENTIRE AFFECTED AREA WITH ONE APPLICATION
  • GRADUALLY INCREASE TO 2 OR 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR
  • IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION TO EVERY OTHER DAY.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER , BUTYLENE GLYCOL , CETYL ESTERS , STEARIC ACID , KAOLIN , GLYCERYL DILAURATE , HYDROGENATED POLYISOBUTENE , STEARETH-21 , LAMINARIA SACCHARINA EXTRACT , CAFFEINE , PEG-150 PENTAERYTHRITYL TETRASTEARATE , STEARETH-2 , GLYCERYL STEARATE , LECITHIN , ACETYL GLUCOSAMINE , CELLULOSE GUM , 10-HYDROXYDECANOIC ACID , MAGNESIUM ALUMINUM SILICATE, , SILICA , XANTHAN GUM , AMINOMETHYL PROPANEDIOL , SIMETHICONE , TOCOPHERYL ACETATE , DISODIUM EDTA , PHENOXYETHANOL , POTASSIUM SORBATE  MAY CONTAIN: MICA, TITANIUM DIOXIDE, IRON OXIDES, CHROMIUM OXIDE GREENS  ILN35126

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


PRINCIPLE DISPLAY PANEL   0.34 FL OZ LIQ CARTON

CLINIQUE ACNE SOLUTIONS CLEARING CONCEALER
SALICYLIC ACID ACNE MEDICATION

ALL SKIN TYPES

.34 FL OZ/ 10 mL


CLINIQUE LABS DISTR.
NEW YORK, NY 10022
CLINIQUE.COM

FOLDING CARTON
FOLDING CARTON



DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
245199salicylic acid 1 % Topical LotionPSN1
245199salicylic acid 10 MG/ML Topical LotionSCD1
245199salicylic acid 1 % Topical LotionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49527-749-012020-01-31C16284748780-19d75b9d0-307c-f424-e053-dadaa90a57ceaed2f50e-123a-43e2-8e9a-e02c657bcc12

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49527-749-01ACNE SOLUTIONS CLEARING CONCEALERACNE MEDICATION ALL SKIN TYPES1 in 1 CARTONLOTION11
49527-749-02ACNE SOLUTIONS CLEARING CONCEALERACNE MEDICATION ALL SKIN TYPES10 mL in 1 TUBELOTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49527-749ACNE SOLUTIONS CLEARING CONCEALER ACNE MEDICATION ALL SKIN TYPES (SALICYLIC ACID) LOTION [CLINIQUE LABORATORIES INC]1Legacy NDC, 2 package rows20100402_aed2f50e-123a-43e2-8e9a-e02c657bcc12.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
49527-74949527-749-02, 49527-749-01

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
8cfbc730-2097-4261-9011-1c76ba1a31a3aed2f50e-123a-43e2-8e9a-e02c657bcc122010-04-01WarningsExact identifier
spl id: 8cfbc730-2097-4261-9011-1c76ba1a31a3
spl set id: aed2f50e-123a-43e2-8e9a-e02c657bcc12

Reported adverse events (FAERS/openFDA)#

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