FDA.reportPublic FDA data

SALICYLIC ACID

Manufacturer
S+
Effective date
2023-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:16:41

Label at a glance#

ProductCLEAR AND COVER ACNE TREATMENT CONCEALER CLEAR AND COVER ACNE TREATMENT CONCEALER 10 walnut
Active ingredientSALICYLIC ACID
Label structure6 sections

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 becaused excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three tiems 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 ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Use

INDICATIONS & USAGE SECTION

  • for the treatment of acne
  • clears acne blemishes
  • helps prevent new acne blemishes

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

  • clean the skin thoroughly before applying this product
  • cover the entire affected area with a thin layer one to three times daily
  • becaused excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three tiems 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 (Aqua), Cyclopentasiloxane, Butylene Glycol, Dimethicone, Trisiloxane, Kaolin, Polyisobutene, PEG/PPG-18/18 Dimethicone, Boron Nitride, Talc, Cyclodextrin, Cetyl PEG/PPG-10/1 Dimethicone, Disteardimonium Hectorite, Magnesium Sulfate, Methyl Methacrylate Crosspolymer, Trimethylsiloxysilicate, Phenoxyethanol, Bisabolol, Caprylyl Glycol, Glycerin, Triethoxycaprylylsilane, Tocopherol, Chamomilla Recutita (Matricaria) Flower Extract, Tocopheryl Acetate, Alumina, Silica, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate.
May Contain (+/-): Zinc Oxide (CI 77947), Titanium Dioxide (CI 77891), Iron Oxides (CI 77491/CI 77492/CI 77499).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Packagewalnutwalnut

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
31720-96031720-960-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIMETHICONE92RU3N3Y1OIACT
TRISILOXANE9G1ZW13R0GIACT
KAOLIN24H4NWX5COIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
BORON NITRIDE2U4T60A6YDIACT
TALC7SEV7J4R1UIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMEREG97988M5QIACT
PHENOXYETHANOLHIE492ZZ3TIACT
LEVOMENOL24WE03BX2TIACT
CAPRYLYL GLYCOL00YIU5438UIACT
GLYCERINPDC6A3C0OXIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
TOCOPHEROLR0ZB2556P8IACT
CHAMOMILEFGL3685T2XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALUMINUM OXIDELMI26O6933IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
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
1998ddd2-909f-128b-e063-6294a90a7b3bddbb2ebd-63ef-4b85-9acb-088179e658ed2024-05-29WarningsExact identifier
spl set id: ddbb2ebd-63ef-4b85-9acb-088179e658ed

Reported adverse events (FAERS/openFDA)#

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