FDA.reportPublic FDA data

Evenly Plus Psoriasis care

Manufacturer
Evenly Plus, Inc
Effective date
2017-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:26

Label at a glance#

ProductEvenly Plus Psoriasis care
Active ingredientSALICYLIC ACID
Label structure6 sections

Indications and uses

For relief or controls for the symptoms of psoriasis.

Dosage and administration

Cleanse the skin thoroughly before applying medication Cover the entire affected area with a thin layer one tothree times a day. Because excessive drying of the skin may occur, start with one application daily, then gradually increaseto 2 to 3 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 2.00%

Purpose

OTC - PURPOSE SECTION

Psoriasis treatment

Uses:

INDICATIONS & USAGE SECTION

For relief or controls for the symptoms of psoriasis.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you have very sensitive skin or are sensitive to Salicylic Acid

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. If this happens, rinse thoroughly with water.

  • If condition worsenson does not improve after regular use of this product as directed, consult a physician.
  • Use caution in exposing skin to sunlight after applying this product. If may increase your tendency to sunburn for up to 24 hours after application.
  • If condition covers a large area of the body, consult your physician before using this product.

Stop and ask a doctor if 

OTC - STOP USE SECTION

irritation becomes severe

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

  • Cleanse the skin thoroughly before applying medication
  • Cover the entire affected area with a thin layer one tothree times a day. Because excessive drying of the skin may occur, start with one application daily, then gradually increaseto 2 to 3 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

Cocos Nucifera (Coconut) Oil. Parfum (Fragrance), Olea Europea (Olive) Oil, Paraffin Wax, Theobroma Cacao (Cocoa) Butter, Tocopheryl Acetate (Vitamin E).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label7Label7

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71802-85671802-856-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCONUT OILQ9L0O73W7LIACT
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLESXO45V955LTIACT
PARAFFINI9O0E3H2ZEIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
0722e7dc-80e7-2a72-e063-6294a90a543014d9bbf7-9e84-4ae2-88f2-6c062889723b2023-10-07WarningsExact identifier
spl set id: 14d9bbf7-9e84-4ae2-88f2-6c062889723b

Reported adverse events (FAERS/openFDA)#

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