FDA.reportPublic FDA data

ClearSkinDays Acne Clearing Drops

Manufacturer
Sephora Usa, Inc
Effective date
2020-08-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:59

Label at a glance#

ProductClearSkinDays Acne Clearing Drops
Active ingredientSALICYLIC ACID
Label structure8 sections

Indications and uses

for the treatment of acne

Dosage and administration

clean the skin thoroughly before applying this product 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

Label contents#

Full prescribing information#

Active ingredients

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

Avoid contact with eyes

if contact occurs, flush thoroughly with water

Other information

SPL UNCLASSIFIED SECTION

avoid storing at extreme temperatures (below 40°F and above 100°F)

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the skin thoroughly before applying this product
  • 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 ingredients

INACTIVE INGREDIENT SECTION

water, propanediol, niacinamide, hydroxyethylcellulose, sodium hydroxide, zinc PCA, phenoxyethanol, ethylhexylglycerin, trisodium ethylenediamine disuccinate

Questions or Comments?

OTC - QUESTIONS SECTION

1-877-SEPHORA (1-877-737-4672)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68469-01468469-014-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
NIACINAMIDE25X51I8RD4IACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
SODIUM HYDROXIDE55X04QC32IIACT
ZINC PIDOLATEC32PQ86DH4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TRISODIUM ETHYLENEDIAMINE DISUCCINATEYA22H34H9QIACT
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
09d004ba-518d-2a21-e063-6394a90acba5bba2537e-9914-4ab1-bd2d-92745708a9e72023-11-10WarningsExact identifier
spl set id: bba2537e-9914-4ab1-bd2d-92745708a9e7

Reported adverse events (FAERS/openFDA)#

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