PSORIASIS RELIEF CREAM

Manufacturer
Nerium SkinCare, Inc. | Chemolee Lab Corporation
Effective date
2018-04-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:00:03

Label at a glance#

ProductPSORIASIS RELIEF
Active ingredientSALICYLIC ACID
Label structure9 sections

Indications and uses

Controls and helps prevent recurrence of skin itching, irritation, redness, flaking and scaling associated with seborrheic dermatitis, and or psoriasis.

Dosage and administration

Apply to affected areas one to four times daily or as directed by a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

SALICYLIC ACID 2.0%

PURPOSE

OTC - PURPOSE SECTION

PSORIASIS/SEBORRHEIC DERMATITIS CREAM

USES

INDICATIONS & USAGE SECTION

  • Controls and helps prevent recurrence of skin itching, irritation, redness, flaking and scaling associated with seborrheic dermatitis, and or psoriasis.

WARNINGS

WARNINGS SECTION

For external use only
Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
If condition worsens or does not improve after regular use of this product as directed, consult a doctor.
If condition covers a large area of the body, consult your doctor before using this product.

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

  • Apply to affected areas one to four times daily or as directed by a doctor.

OTHER INGREDIENTS

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Nerium Oleander Leaf Extract (NAE-8®), Water (Aqua), Propanediol, Hydrolyzed Egg Shell Membrane (BiovaDerm®), Cetyl Alcohol, Glycerin, Glyceryl Stearate, Potassium Cetyl Phosphate, Cetearyl Olivate, Caprylic/Capric Triglyceride, Dimethicone, Ricinus Communis (Castor) Seed Oil, Glyceryl Caprylate, Sorbitan Olivate, Lysolecithin, Sclerotium Gum, Xanthan Gum, Allantoin, Arginine, Avena Sativa Kernel Flour (Colloidal Oatmeal), Butyrospermum Parkii (Shea) Butter, Olea Europaea (Olive) Fruit Oil, Pelargonium Graveolens Flower Oil, Tocopherol, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Pullulan, Ocimum Basilicum (Basil) Extract, Linum Usitatissimum (Linseed) Seed Oil, Carum Petroselinum (Parsley) Extract, Benzyl Alcohol, Potassium Sorbate, Dipotassium Glycyrrhizate, Glyceryl Undecylenate, Sea Salt, Mahonia Aquifolium (Oregon Grape) Root Extract, Sodium Benzoate, Muriella Aurantiaca/Ruttnera Lamellosa Oil (Plankton Extract), Citric Acid, Lecithin

QUESTIONS?

OTC - QUESTIONS SECTION

1-(844)-599-7787 M-F (9 am to 5 pm CST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NSC.Psoriasis.Carton.30ml.V21_RevisedNSC.Psoriasis.Carton.30ml.V21_Revised

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72216-101-112023-04-06C16284748780-1d6a99b39-9cdf-a426-e053-dadaa90af4c2PSORIASIS RELIEF CREAM
72216-101-112022-01-28C16284748780-1d6a99b39-9cdf-a426-e053-dadaa90af4c2PSORIASIS RELIEF CREAM

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72216-10172216-101-01, 72216-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 41 matching rows.

Source Document#

Source XML · Source PDF

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
f8b0d036-7ac4-99e7-e053-6394a90a5d3e5fcb1e6d-e109-4ded-b15a-a4484de784192023-04-06WarningsExact identifier
spl set id: 5fcb1e6d-e109-4ded-b15a-a4484de78419

Reported adverse events (FAERS/openFDA)#

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