Psoriasin Daytime Relief

Manufacturer
Alva-Amco Pharmacal Companies, Inc.
Effective date
2018-12-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:42:33

Label at a glance#

ProductPsoriasin Daytime Relief
Active ingredientCOAL TAR
Label structure13 sections

Indications and uses

For the relief of symptoms associated with psoriasis and/or seborrheic dermatitis including itching, scaling, flaking, redness and irritation of the skin. Helps prevent recurrence.

Dosage and administration

Read all package directions and warnings before use. Use only as directed. Apply (gently massage in) a small amount of Psoriasin to affected areas. Apply one to four times daily or as directed by a doctor. Apply to thoroughly dry skin. The active ingredient, coal tar, in Psoriasin, may affect very light hair color; test first on a few strands of hair before broader application to areas where light-colored hair is ...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Coal tar (from coal tar topical solution, USP 20%) 1.25%

Purpose

OTC - PURPOSE SECTION

Psoriasis/Seborrheic Dermatitis Treatment

Uses

INDICATIONS & USAGE SECTION

For the relief of symptoms associated with psoriasis and/or seborrheic dermatitis including itching, scaling, flaking, redness and irritation of the skin. Helps prevent recurrence.

Warnings

WARNINGS SECTION

For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctor before use

  • for prolonged periods
  • if condition covers a large area of the body
  • around the rectum or in the genital area or groin
  • with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • condition does not improve after regular use of this product as directed.

Use caution in exposing skin to sunlight after applying this product, as it may increase your tendency to sunburn for up to 24 hours after application.

Warning:  This product contains chemicals known to the State of California to cause cancer.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Read all package directions and warnings before use.
  • Use only as directed.
  • Apply (gently massage in) a small amount of Psoriasin to affected areas.
  • Apply one to four times daily or as directed by a doctor.
  • Apply to thoroughly dry skin.
  • The active ingredient, coal tar, in Psoriasin, may affect very light hair color; test first on a few strands of hair before broader application to areas where light-colored hair is present.
  • Wash affected area at least daily with mild soap and warm ater and dry thoroughly.
  • Intended for use by normally healthy adults only.
  • Persons under 18 years of age or those with highly sensitive or allergic skin should use only as directed by a doctor.

Other information

INFORMATION FOR PATIENTS SECTION

You may report serious side effectes to the phone number provided under Questions? below.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis leaf juice, Bromelain, Butyrospermum Parkii (shea) butter, Caprylic/capric triglyceride, Ceteareth-20, Cetearyl alcohol, Cetyl alcohol, Chamomilla Recutita (Matricaria) flower extract, Cholecalciferol, Colloidal oatmeal, Dimethicone, Ethanol, Ethylhexylglycerin, Glycerin, Glycerol stearate, PEG-100 stearate, Persea Gratissima (avocado) oil, Phenoxyethanol, Polysorbate 80, Propylene glycol, Tocopheryl acetate, Urea, Water and Zea mays (corn) oil.

OTC - QUESTIONS SECTION

Questions? 1-800-792-2582

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PsoriasinDaytimePDPPsoriasinDaytimePDP

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52389-74552389-745-01, 52389-745-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

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
7cef4576-6a2a-8fc2-e053-2a91aa0a8c3422ca9abf-8f1d-4fc6-9733-38f1c0cecfc12018-12-13WarningsExact identifier
spl id: 7cef4576-6a2a-8fc2-e053-2a91aa0a8c34
spl set id: 22ca9abf-8f1d-4fc6-9733-38f1c0cecfc1

Reported adverse events (FAERS/openFDA)#

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