MG217 Psoriasis

Manufacturer
Wisconsin Pharmacal Company
Effective date
2016-03-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:45:19

Label at a glance#

ProductMG217 Psoriasis
Active ingredientSALICYLIC ACID
Label structure11 sections

Indications and uses

For the relief of itching, scaling, redness, flaking and irritation associated with psoriasis and/or seborrheic dermatitis. Helps prevents symptom recurrence.

Dosage and administration

Apply to affected area 1 to 4 times daily, or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 3%

Purpose

OTC - PURPOSE SECTION

Psoriasis/Seborrheic Dermatitis Treatment

Uses

INDICATIONS & USAGE SECTION

For the relief of itching, scaling, redness, flaking and irritation associated with psoriasis and/or seborrheic dermatitis. Helps prevents symptom recurrence.

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 immediately.

Warnings

WARNINGS SECTION

For external use only.

Avoid contact with the eyes If contact occurs, rinse eyes thoroughly with water.

Consult a doctor

OTC - ASK DOCTOR SECTION

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

Consult a doctor before use if condition covers a large area of the body.

Other information

OTHER SAFETY INFORMATION

Keep cap tightly closed when not in use. Store at room temperature.

Questions or comments?

OTC - QUESTIONS SECTION

1-800-635-3696

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area 1 to 4 times daily, or as directed by a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, Glycerin, Cetyl alcohol, Corn starch, Persea gratissima (Avocado) oil, Cetearyl alcohol, Dicetyl phosphate, Ceteth-10 phophate, Cyclosiloxane blend, PEG-40 Stearate, Butyrospermum parkii (Shea) butter, Isopropyl myristate, Lanolin oil, Mahonia Aquifolium (Oregon-grape root), Sodium PCA, Sodium hydroxide, Aloe vera, C12-15 Alkyl benzoate, Glycyrrhizic acid (Licorice extract), Phenoxyethanol, Methyl paraben, n-Butyl paraben, Ethyl paraben, Isobutyl paraben, Propyl paraben, a-Bisabolol, N,2,3-Trimethyl-2-Isopropylbutamide, Allantoin, D-Panthenol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCartonTubeTube

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68093-7203-1MG217 Psoriasis1 in 1 CARTONSHAMPOO12
68093-7203-1MG217 Psoriasis104 g in 1 TUBESHAMPOO1042

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68093-7203MG217 PSORIASIS (SALICYLIC ACID) SHAMPOO [WISCONSIN PHARMACAL COMPANY]2Current NDC, Legacy NDC, 2 package rows20160304_2d2c2ab3-7c9e-1d09-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68093-720368093-7203-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
MG217 PsoriasisSALICYLIC ACIDWisconsin Pharmacal Company2d2c2ab3-7c9e-1d09-e054-00144ff8d46c2016-03-03WarningsExact identifier
ndc (package): 68093-7203-1
ndc (product): 68093-7203
ndc11 (package): 68093720301
spl id: 244a1452-5d59-3219-e054-00144ff88e88
spl set id: 2d2c2ab3-7c9e-1d09-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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