FDA.reportPublic FDA data

Clarisonic Pore and Blemish Cleanser Acne Treatment

Manufacturer
Pacific Bioscience Laboratories, Inc. | L'Oreal USA, Inc.
Effective date
2023-12-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:16:47

Label at a glance#

ProductClarisonic Pore and Blemish Cleanser Acne Treatment
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

for the treatment of acne

Dosage and administration

apply directly to moistened skin or to a damp Clarisonic skin cleansing brush massage onto face, avoiding the eye area rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Uses

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply directly to moistened skin or to a damp Clarisonic skin cleansing brush
  • massage onto face, avoiding the eye area
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium laureth sulfate, decyl glucoside, glycerin, sodium chloride, coco-betaine, PEG-150 pentaerythrityl tetrastearate, PEG-6 caprylic/capric glycerides, zinc gluconate, sodium hydroxide, sodium benzoate, tetrasodium EDTA, capryloyl salicylic acid, citric acid, menthol, hexylene glycol, polyquaternium-47

Questions?

OTC - QUESTIONS SECTION

Call 1-888-525-2747

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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
69481-33369481-333-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
DECYL GLUCOSIDEZ17H97EA6YIACT
GLYCERINPDC6A3C0OXIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCO-BETAINE03DH2IZ3FYIACT
PEG-150 PENTAERYTHRITYL TETRASTEARATE8L4OOQ76AMIACT
PEG-6 CAPRYLIC/CAPRIC GLYCERIDESGO50W2HWO8IACT
ZINC GLUCONATEU6WSN5SQ1ZIACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM BENZOATEOJ245FE5EUIACT
EDETATE SODIUMMP1J8420LUIACT
CAPRYLOYL SALICYLIC ACID5F7PJF6AA4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
MENTHOLL7T10EIP3AIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
POLYQUATERNIUM-47 (METHACRYLAMIDOPROPYLTRIMETHYLAMMONIUM CHLORIDE-CO-METHYL ACRYLATE-CO-ACRYLIC ACID 45:10:45; 1200000 MW)F11YNO8FDQIACT

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
a020aafe-45f3-4bdf-a910-f54c81709979c786f377-0b2f-4288-833b-a52ae633a2d92023-12-27WarningsExact identifier
spl id: a020aafe-45f3-4bdf-a910-f54c81709979
spl set id: c786f377-0b2f-4288-833b-a52ae633a2d9

Reported adverse events (FAERS/openFDA)#

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