FDA.reportPublic FDA data

Clear Skin Days Spot Eraser Stick

Manufacturer
Sephora Usa, Inc
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:48:35

Label at a glance#

ProductClear Skin Days Spot Eraser Stick
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

Alcohol denat. (SD Alcohol 40-B), allantoin, betaine, glycerin, Mexican giant hyssop (Agastache mexicana) flower/leaf/stem extract, phenoxyethanol, propanediol, sodium gluconate, sodium hydroxide, water.

Questions or Comments?

OTC - QUESTIONS SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package3Outer Package3Inner Package3Inner Package3

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
68469-01268469-012-10

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
ALCOHOL3K9958V90MIACT
ALLANTOIN344S277G0ZIACT
BETAINE3SCV180C9WIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPANEDIOL5965N8W85TIACT
SODIUM GLUCONATER6Q3791S76IACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
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
09cfb6ca-9626-0f26-e063-6394a90a2ff9d09f2784-9be4-4ca5-80e3-bc47a1cacef22023-11-10WarningsExact identifier
spl set id: d09f2784-9be4-4ca5-80e3-bc47a1cacef2

Reported adverse events (FAERS/openFDA)#

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